US20180362460A1 - Cyanopyrrolidine derivatives as inhibitors for dubs - Google Patents

Cyanopyrrolidine derivatives as inhibitors for dubs Download PDF

Info

Publication number
US20180362460A1
US20180362460A1 US16/060,299 US201616060299A US2018362460A1 US 20180362460 A1 US20180362460 A1 US 20180362460A1 US 201616060299 A US201616060299 A US 201616060299A US 2018362460 A1 US2018362460 A1 US 2018362460A1
Authority
US
United States
Prior art keywords
optionally substituted
cyano
carboxamide
ring
alkyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
US16/060,299
Other versions
US10590075B2 (en
Inventor
Mark Ian Kemp
Michael David Woodrow
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mission Therapeutics Ltd
Original Assignee
Mission Therapeutics Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mission Therapeutics Ltd filed Critical Mission Therapeutics Ltd
Assigned to MISSION THERAPEUTICS LIMITED reassignment MISSION THERAPEUTICS LIMITED ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KEMP, MARK IAN, WOODROW, MICHAEL DAVID
Publication of US20180362460A1 publication Critical patent/US20180362460A1/en
Application granted granted Critical
Publication of US10590075B2 publication Critical patent/US10590075B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Definitions

  • the present invention relates to novel compounds and methods for the manufacture of inhibitors of deubiquitylating enzymes (DUBs).
  • the invention relates to the inhibition of Cezanne 1.
  • the invention further relates to the use of DUB inhibitors in the treatment of cancer.
  • Ubiquitin is a small protein consisting of 76 amino acids that is important for the regulation of protein function in the cell.
  • Ubiquitylation and deubiquitylation are enzymatically mediated processes by which ubiquitin is covalently bound or cleaved from a target protein. These processes have been implicated in the regulation of many cellular functions including cell cycle progression, apoptosis, modification of cell surface receptors, regulation of DNA transcription and DNA repair.
  • the ubiquitin system has been implicated in the pathogenesis of numerous disease states including inflammation, viral infection, metabolic dysfunction, CNS disorders, and oncogenesis.
  • Ubiquitin molecules are cleaved from proteins by deubiquitylating enzymes (DUBs), of which there are approximately 95 DUBs in human cells, divided into sub-families based on sequence homology.
  • DUBs deubiquitylating enzymes
  • the ovarian tumour (OTU) family consists of at least 14 active DUBs and are characterised by the presence of an OTU domain and the tendency to cleave ubiquitin chains in a linkage specific manner.
  • Cezanne 1 also known as OTUD7B, is an 843 amino acid protein that was identified owing to its similarity to the OTU family member A20 that has been shown biochemically to have a strong preference for K11 ubiquitin chain linkages.
  • Cezanne 1 has been shown to act as a negative regulator of both the canonical and the non-canonical NF- ⁇ B pathway. It has been shown that Cezanne 1 acts on the canonical pathway by processing K63 chains on the RIP 1 protein and on the non-canonical pathway by deubiquitylation of the inhibitory component TRAF3 (TNF receptor associated factor 3). It has also been shown to have a role in hypoxia by regulating HIF1 ⁇ (hypoxia inducible factor 1 ⁇ ) protein levels. Cezanne 1 siRNA decreased HIF1 ⁇ protein levels under hypoxia, and accordingly decreased HIF1 ⁇ target gene expression. Knockdown of Cezanne 1 led to higher levels of apoptosis following hypoxia. Since HIF1 ⁇ has oncogenic properties, and Cezanne 1 has a pro-survival role in hypoxia, Cezanne 1 has been suggested to be a good target for pharmacological intervention.
  • HIF1 ⁇ has oncogenic properties
  • Cezanne 1 has a pro-survival role in hypo
  • Cezanne 1 has been shown to have a role in cell proliferation, migration and invasion by antagonizing EGFR (epidermal growth factor receptor) internalisation and degradation.
  • Cezanne 1 and Cezanne 2 were identified in a genetic screen to find a DUB enzyme for EGFR.
  • Cezanne 1 overexpression led to higher levels of phosphorylated EGFR, lower levels of ubiquitylated EGFR and EGFR stabilization.
  • knockdown of Cezanne 1 led to decreased invasion and migration.
  • Analysis of The Cancer Genome Atlas by Pareja et al. showed that Cezanne 1 was overexpressed in breast cancer and amplification of the gene was seen in a third of breast tumours. The level of Cezanne 1 expression correlated with poor prognosis.
  • R 1a , R 1b , R 1c and R 1d each independently represent hydrogen or an optionally substituted C 1 -C 6 alkyl, or R 1a is linked to R 1b to form an optionally substituted cycloalkyl ring, or R 1d is linked to R 1c or R 1e to form an optionally substituted cycloalkyl ring;
  • R 1e and R 1f each independently represent hydrogen, fluorine, cyano, hydroxyl, amino, optionally substituted C 1 -C 6 alkyl, optionally substituted C 1 -C 6 alkoxy or an optionally substituted 5 or 6 membered aryl or heteroaryl ring, or R 1e and R 1f together form an optionally substituted cycloalkyl ring, or R 1e is linked to R 1d to form an optionally substituted cycloalkyl ring;
  • A is an optionally substituted 5 to 10 membered heteroaryl or aryl ring.
  • A may represent a 5 to 10 membered heteroaryl or aryl ring substituted with one or more of Q 1 -(R 2 ) n , wherein:
  • n 0 or 1
  • Q 1 represents halogen, cyano, oxo, nitro, —OR 3 , —SR 3 , —NR 3 R 4 , —CONR 3 R 4 , —NR 3 COR 4 , —NR 3 CONR 4 R 5 , —COR 3 , —C(O)OR 3 , —SO 2 R 3 , —SO 2 NR 3 R 4 , —NR 3 SO 2 R 4 , —NR 3 SO 2 NR 4 R 5 , —NR 3 C(O)OR 4 , optionally substituted —C 1 -C 6 alkyl, optionally substituted —C 1 -C 6 alkoxy, optionally substituted —C 2 -C 6 alkenyl, optionally substituted —C 2 -C 6 alkynyl, a covalent bond, an oxygen atom, a sulphur atom, —SO—, —SO 2 —, —CO—, —C(O)O—, —
  • R 3 , R 4 and R 5 each independently represent hydrogen, optionally substituted C 1 -C 6 alkyl or optionally substituted C 1 -C 6 alkylene.
  • R 2 represents an optionally substituted 3 to 10 membered heterocyclyl, heteroaryl, aryl or cycloalkyl ring. (When n is 0, Q 1 is present and R 2 is absent).
  • R 2 may be optionally substituted with one or more substituents selected from halogen, cyano, oxo, nitro, —OR 6 , —SR 6 , —NR 6 R 7 , —CONR 6 R 7 , —NR 6 COR 7 , —NR 6 CONR 7 R 8 , —COR 6 , —C(O)OR 6 , —SO 2 R 6 , —SO 2 NR 6 R 7 , —NR 6 SO 2 R 7 , —NR 6 SO 2 NR 7 R 8 , —NR 6 C(O)OR 7 , optionally substituted —C 1 -C 6 alkyl, optionally substituted —C 1 -C 6 alkoxy, optionally substituted —C 2 -C 6 alkenyl, optionally substituted —C 2 -C 6 alkynyl, -Q 2 -R 6 , -Q 2 -NR 6 CONR 7 R 8 , -Q 2 -NR 6 R
  • Q 2 represents a covalent bond, an oxygen atom, a sulphur atom, —SO—, —SO 2 —, —CO—, optionally substituted C 1 -C 6 alkylene or optionally substituted C 2 -C 6 alkenylene;
  • R 6 , R 7 , R 8 each independently represent hydrogen, optionally substituted C 1 -C 6 alkyl, optionally substituted heterocyclyl, optionally substituted heteroaryl, optionally substituted aryl, or an optionally substituted cycloalkyl.
  • the invention also relates to pharmaceutical compositions comprising the compounds of the present invention and one or more pharmaceutically acceptable excipients.
  • the compounds of the invention are useful for the treatment of cancer.
  • FIG. 1 provides an image of Cezanne 1 purified from mammalian cells. FLAG-purified protein or the indicated concentrations of BSA were separated by SDS-PAGE and stained with Imperial (Pierce Biotechnology).
  • FIG. 2 is a graph showing proteolytic activity of Cezanne 1 measured using a fluorescence polarisation assay. Various volumes of purified Cezanne 1 as indicated were incubated with a TAMRA labelled peptide linked to ubiquitin via an isopeptide bond.
  • any group of the compounds of formula (I) have been referred to as optionally substituted, this group may be substituted or unsubstituted. Substitution may be by one or more of the specified substituents which may be the same or different. It will be appreciated that the number and nature of substituents will be selected to avoid any sterically undesirable combinations.
  • alkyl, alkylene, alkoxy, alkenyl, or alkynyl substituent (or linker) group or an alkyl, alkenyl moiety in a substituent group may be linear or branched.
  • Alkyl, alkylene, alkenyl and alkenylene chains may also include intervening heteroatoms such as oxygen.
  • C x -C y alkyl refers to a saturated aliphatic hydrocarbon group having x-y carbon atoms which may be linear or branched.
  • C 1 -C 6 alkyl contains from 1 to 6 carbon atoms and includes C 1 , C 2 , C 3 , C 4 , C 5 and C 6 .
  • “Branched” means that at least one carbon branch point is present in the group. For example, tert-butyl and isopropyl are both branched groups.
  • C 1 -C 6 alkyl groups include methyl, ethyl, propyl, 2-methyl-1-propyl, 2-methyl-2-propyl, 2-methyl-1-butyl, 3-methyl-1-butyl, 2-methyl-3-butyl, 2,2-dimethyl-1-propyl, 2-methyl-pentyl, 3-methyl-1-pentyl, 4-methyl-1-pentyl, 2-methyl-2-pentyl, 3-methyl-2-pentyl, 4-methyl-2-pentyl, 2,2-dimethyl-1-butyl, 3,3-dimethyl-1-butyl, 2-ethyl-1-butyl, n-butyl, isobutyl, tert-butyl, n-pentyl, isopentyl, neopentyl and n-hexyl.
  • substituted C 1 -C 6 alkyl therefore include CF 3 , CH 2 CF 3 , CH 2 CN, CH 2 OH and CH 2 CH 2 OH.
  • a C x -C y alkylene group or moiety may be linear or branched and refers to a divalent hydrocarbon group having one less hydrogen atom from C x -C y alkyl as defined above.
  • C 1 -C 6 alkylene may include intervening heteroatoms such as oxygen, and therefore includes alkyleneoxy groups.
  • Alkyleneoxy as employed herein also extends to embodiments in which the or an oxygen atom (e.g. a single oxygen atom) is located within the alkylene chain, for example CH 2 CH 2 OCH 2 or CH 2 OCH 2 .
  • C 1 -C 6 alkylene groups include methylene, methyleneoxy, ethylene, ethyleneoxy, n-propylene, n-propyleneoxy, n-butylene, n-butyleneoxy, methylmethylene and dimethylmethylene.
  • C 1 -C 6 alkylene, C 1 -C 4 alkylene and C 1 -C 3 alkylene within the definitions of R 3 , R 4 , R 5 , Q 1 and Q 2 may be unsubstituted or substituted with one or more of the substituents defined herein.
  • C 2 -C 6 alkenyl refers to a linear or branched hydrocarbon chain radical containing at least two carbon atoms and at least one double bond and includes C 2 -C 4 alkenyl.
  • alkenyl groups include ethenyl, propenyl, 2-propenyl, 1-butenyl, 2-butenyl, 1-hexenyl, 2-methyl-1-propenyl, 1,2-butadienyl, 1,3-pentadienyl, 1,4-pentadienyl and 1-hexadienyl.
  • C 2 -C 6 alkenyl and C 2 -C 4 alkenyl within the definitions of Q 1 and within the definition of substituents for R 2 may be unsubstituted or substituted with one or more of the substituents defined herein.
  • C 2 -C 6 alkenylene refers to linear or branched hydrocarbon group having one less hydrogen atom from C 2 -C 6 alkenyl as defined above.
  • Examples of C 2 -C 6 alkenylene include ethenylene, propenylene and butenylene.
  • C 2 -C 6 alkenylene and C 2 -C 4 alkenylene within the definition of substituents for Q 1 and Q 2 may be unsubstituted or substituted with one or more of the substituents defined herein.
  • C 2 -C 6 alkynyl refers to a linear or branched hydrocarbon chain radical containing at least two carbon atoms and at least one triple bond.
  • alkenyl groups include ethynyl, propynyl, 2-propynyl, 1-butynyl, 2-butynyl and 1-hexynyl.
  • C 2 -C 6 alkynyl, within the definitions of Q 1 and within the definition of substituents for R 2 may be unsubstituted or substituted with one or more of the substituents defined herein.
  • C 1 -C 6 alkoxy refers to a group or part of a group having an —O—C x -C y alkyl group according to the definition of C x -C y alkyl above.
  • C 1 -C 6 alkoxy contains from 1 to 6 carbon atoms and includes C 1 , C 2 , C 3 , C 4 , C 5 and C 6 .
  • Examples of C 1 -C 6 alkoxy include methoxy, ethoxy, propoxy, isopropoxy, butoxy, pentoxy and hexoxy.
  • Alkoxy as employed herein also extends to embodiments in which the or an oxygen atom (e.g.
  • a single oxygen atom is located within the alkyl chain, for example CH 2 CH 2 OCH 3 or CH 2 OCH 3 .
  • the alkoxy may be linked through carbon to the remainder of the molecule, for example, —CH 2 CH 2 OCH 3 , or alternatively, the alkoxy is linked through oxygen to the remainder of the molecule, for example —OC 1-6 alkyl.
  • the alkoxy may be linked through oxygen to the remainder of the molecule but the alkoxy group contains a further oxygen atom, for example —OCH 2 CH 2 OCH 3 .
  • C 1 -C 6 alkoxy and C 1 -C 3 alkoxy within the definitions R 1e , R 1f , Q 1 , and within the definition of substituents for R 2 may be unsubstituted or substituted with one or more of the substituents defined herein.
  • substituted C 1 -C 6 alkoxy therefore include OCF 3 , OCHF 2 , OCH 2 CF 3 , CH 2 CH 2 OCH 3 and CH 2 CH 2 OCH 2 CH 3 .
  • halogen refers to chlorine, bromine, fluorine or iodine atoms, in particular chlorine or fluorine atoms.
  • cycloalkyl, heterocyclyl, aryl and heteroaryl rings disclosed herein and within the definitions of R 1a , R 1b , R 1c , R 1d , R 1e , R 1f , R 2 , R 6 , R 7 , R 8 , ring A, and within the definition of substituents for R 2 do not include any unstable ring structures or, in the case of heteroaryl and heterocyclic rings systems, any O—O, O—S or S—S bonds.
  • the ring systems may be monocyclic or bicyclic. Bicyclic ring systems include bridged, fused and spiro ring systems.
  • a substituent if present may be attached to any suitable ring atom which may be a carbon atom or, in the case of heteroaryl and heterocyclic ring systems, a heteroatom.
  • Substitution on a ring may also include a change in the ring atom at the position of the substitution.
  • substitution on a phenyl ring may include a change in the ring atom at the position of substitution from carbon to nitrogen, resulting in a pyridine ring.
  • cycloalkyl refers to a monocyclic saturated or partially unsaturated, non-aromatic ring, wherein all of the ring atoms are carbon, and having the number of ring atoms as indicated.
  • C 3 -C 10 cycloalkyl refers to a monocyclic or bicyclic hydrocarbon ring containing 3 to 10 carbon atoms.
  • Examples of C 3 -C 10 cycloalkyl are cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl and decahydronaphthalenyl.
  • Bicyclic cycloalkyl groups include bridged ring systems such as bicycloheptane and bicyclooctane. Unless specified otherwise, cycloalkyl within the definitions of R 1a , R 1b , R 1c , R 1d , R 1e , R 1f , R 2 , R 6 , R 7 , R 8 , and within the definition of substituents for R 2 , may be unsubstituted or substituted with one or more of the substituents defined herein.
  • aryl group/moiety refers to any monocyclic or bicyclic hydrocarbon group comprising at least one aromatic group and having from 5 to 10 carbon atom ring members.
  • aryl groups include phenyl and naphthyl.
  • Bicyclic rings may be fused aromatic rings where both rings are aromatic, for example, naphthalenyl.
  • Preferred aryl groups are phenyl and naphthyl, more preferably 5 phenyl.
  • aryl within the definitions of R 1e , R 1f , R 2 , R 6 , R 7 , R 8 , ring A, and within the definition of substituents for R 2 may be unsubstituted or substituted with one or more of the substituents defined herein.
  • Heteroaryl as used herein means a polyunsaturated, monocyclic or bicyclic 5 to 10 membered aromatic moiety containing at least one and up to 5 heteroatoms, particularly 1, 2 or 3 heteroatoms selected from N, O and S, and the remaining ring atoms are carbon atoms, in stable combinations known to the skilled person. Heteroaryl ring nitrogen and sulphur atoms are optionally oxidised, and the nitrogen atom(s) are optionally quaternized.
  • a heteroaryl ring can be a single aromatic ring or a fused bicyclic ring where the bicyclic ring system can be aromatic, or one of the fused rings is aromatic and the other is at least partially saturated.
  • a bicyclic heteroaryl is one in which the entire fused ring system is aromatic.
  • fused rings where one of the rings is aromatic and the other is at least partially saturated include tetrahydropyridopyrazinyl, tetrahydroquinolinyl and tetrahydroisoquinolinyl.
  • attachment of the bicyclic ring to the group it is a substituent of relative to the cyanopyrrolidine core, e.g. attachment of ring A via the amide group, is from the aromatic ring of the bicycle.
  • a bicyclic heteroaryl can have the at least one heteroatom in either of the fused rings.
  • a bicyclic ring with an aromatic ring fused to a partially saturated ring may contain the at least one heteroatom in the aromatic ring or the partially saturated ring.
  • Attachment of the bicyclic ring to the group it is a substituent of may be via either a heteroatom containing ring or a carbon only containing ring.
  • the point of attachment of heteroaryl to the group it is a substituent of can be via a carbon atom or a heteroatom (e.g. nitrogen).
  • heteroaryl rings include pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, furyl, pyrrolyl, oxazolyl, thiazolyl, pyrazolyl, triazolyl, tetrazolyl, indolyl, indolizinyl, isoindolyl, purinyl, furazanyl, imidazolyl, indazolyl, isothiazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, thiadiazolyl, benzofuranyl, isobenzofuranyl, benzothiophenyl, isobenzothiophenyl, benzimidazolyl, benzothiazolyl, napthyridinyl, pteridinyl, pyrazinyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazin
  • heteroaryl within the definitions of R 1e , R 1f , R 2 , R 6 , R 7 , R 8 , ring A, and within the definition of substituents for R 2 , may be unsubstituted or substituted with one or more of the substituents defined herein.
  • Heterocyclyl or “heterocyclic” as used herein in describing a ring means, unless otherwise stated, a monocyclic saturated or partially unsaturated, non-aromatic ring or a bicyclic saturated or partially unsaturated ring, wherein the bicyclic ring system is non-aromatic, the mono- or bicyclic ring having, for example, 3 to 10 members, where at least one member and up to 5 members, particularly 1, 2 or 3 members of the ring are heteroatoms selected from N, O and S, and the remaining ring atoms are carbon atoms, in stable combinations known to those of skill in the art.
  • R 2 and R 3 may together form a heterocyclic ring which incorporates the amine nitrogen.
  • Heterocyclic ring nitrogen and sulphur atoms are optionally oxidised, and the nitrogen atoms(s) are optionally quaternized.
  • the heterocyclic ring may be a fused ring to another ring system to form a bicycle, i.e. one or two of the heterocyclic ring carbons is common to an additional ring system.
  • the heterocylcyl is a bicyclic ring
  • the second ring can be aromatic, e.g. a fused phenyl, pyridyl, pyrazolyl, or the like.
  • the bicyclic heterocyclyl can have at least one heteroatom in either of the fused rings.
  • the heterocyclyl may be linked through carbon or a heteroatom to the remainder of the molecule and in instances where the heterocylyl is a bicyclic ring, the link may be via the heteroatom containing ring or the fused ring. In instances where the heterocyclyl is a bicyclic ring where the second ring is aromatic, attachment of the bicyclic group to the group it is a substituent of relative to the cyanopyrrolidine core is from the non-aromatic ring.
  • heterocyclyl groups include azetidinyl, pyrrolidinyl, piperidinyl, azepanyl, diazepanyl, dihydrofuranyl (e.g.
  • heterocyclyl within the definitions of R 2 , R 6 , R 7 , R 8 and within the definition of substituents for R 2 , may be unsubstituted or substituted with one or more of the substituents defined herein.
  • substituted heterocyclyl rings include for example 4,5-dihydro-1H-maleimido,tetramethylenesulfoxide and hydantoinyl.
  • Optionally substituted as applied to any group means that the said group may if desired be substituted with one or more substituents (e.g., 1, 2, 3 or 4 substituents) which may be the same or different.
  • substituents e.g., 1, 2, 3 or 4 substituents
  • substituents for “substituted” and “optionally substituted” C 1 -C 6 alkyl (including C 1 -C 4 alkyl, C 1 -C 3 alkyl and C 1 -C 2 alkyl) and C 1 -C 6 alkoxy (including C 1 -C 4 alkoxy, C 1 -C 3 alkoxy and C 1 -C 2 alkoxy) and C 2 -C 6 alkenyl (including C 2 -C 4 alkenyl) and C 2 -C 6 alkynyl (including C 2 -C 4 alkynyl), for example within the definitions of R 1a , R 1b , R 1c , R 1d , R 1e , R 1f , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , Q 1 , and within the definition of substituents for R 2 , and C 1 -C 6 alkylene (including C 1 -C 3 alkylene) and
  • substituents for “substituted” and “optionally substituted” rings i.e. cycloalkyl, heterocyclyl, aryl and heteroaryl rings, for example within the definitions of R 1a , R 1b , R 1c , R 1d , R 1e , R 1f , R 2 , R 6 , R 7 , R 8 , ring A, and within the definition of substituents for R 2 , include halogen, cyano, oxo, nitro, amino, hydroxy, C 1 -C 6 alkyl or C 1 -C 3 alkyl, C 1 -C 6 alkoxy or C 1 -C 3 alkoxy, aryl, heteroaryl, heterocyclyl, C 3 -C 6 cycloalkyl, C 1-3 alkylamino, C 2-6 alkenylamino, di-C 1 -C 3 alkylamino, C 1 -C 3 acylamino, di-C
  • substituents for “substituted” and “optionally substituted” rings include in particular, fluorine, chlorine, oxo, cyano, C 1 -C 3 alkyl, C 1 -C 3 alkoxy, heterocyclyl, cycloalkyl, heteroary or aryl, wherein the alkyl or alkoxy is optionally substituted with one or more (e.g. one, two or three) substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF 5 .
  • Substituted groups thus include for example Br, Cl, F, CN, Me, Et, Pr, Bu, i-Bu, OMe, OEt, OPr, C(CH 3 ) 3 , CH(CH 3 ) 2 , CF 3 , OCF 3 , C(O)NHCH 3 , cyclopropyl, phenyl, etc.
  • substitutions may be in the form of rings from adjacent carbon atoms in the aryl ring, for example cyclic acetals such as O—CH 2 —O.
  • treat or “treating” or “treatment” includes prophylaxis and means to ameliorate, alleviate symptoms, eliminate the causation of the symptoms either on a temporary or permanent basis, or to prevent or slow the appearance of symptoms of the named disorder or condition.
  • the compounds of the invention are useful in the treatment of humans and non-human animals.
  • the dose of the compound is that amount effective to prevent occurrence of the symptoms of the disorder or to treat some symptoms of the disorder from which the patient suffers.
  • effective amount or “therapeutically effective amount” or “effective dose” is meant that amount sufficient to elicit the desired pharmacological or therapeutic effects, thus resulting in effective prevention or treatment of the disorder.
  • Prevention of the disorder is manifested by delaying the onset of the symptoms of the disorder to a medically significant extent.
  • Treatment of the disorder is manifested by a decrease in the symptoms associated with the disorder or an amelioration of the reoccurrence of the symptoms of the disorder.
  • Pharmaceutically acceptable salts of the compounds of the invention include but are not limited to addition salts (for example phosphates, nitrates, sulphates, borates, acetates, maleates, citrates, fumarates, succinates, methanesulphonates, benzoates, salicylates and hydrohalides), salts derived from organic bases (such as lithium, potassium and sodium), salts of amino acids (such as glycine, alanine, valine, leucine, isoleucine, cysteine, methionine and proline), inorganic bases (such as triethylamine, hydroxide, choline, thiamine and N—N′-diacetylethylenediamine).
  • Other pharmaceutically acceptable salts include ammonium salts, substituted ammonium salts and aluminium salts. Further pharmaceutically acceptable salts include quaternary ammonium salts of the compounds of the invention.
  • salts may be formed by conventional means, for example by reaction of a free acid or a free base form of a compound with one or more equivalents of an appropriate acid or base, optionally in a solvent, or in a medium in which the salt is insoluble, followed by removal of said solvent, or said medium, using standard techniques (e.g. in vacuo, by freeze-drying or by filtration). Salts may also be prepared by exchanging a counter-ion of a compound in the form of a salt with another counter-ion, for example using a suitable ion exchange resin.
  • the invention relates to these compounds prepared as isomeric mixtures or racemates whether present in an optically pure form or as mixtures with other isomers.
  • Enantiomers differ only in their ability to rotate plane-polarized light by equal amounts in opposite directions and are denoted as the (+)/(S) or ( ⁇ )/(R) forms respectively.
  • Individual enantiomers or isomers may be prepared by methods known in the art, such as optical resolution of products or intermediates (for example chiral chromatographic separation e.g. chiral HPLC, or an asymmetric synthesis approach).
  • compounds of the invention exist as alternative tautomeric forms e.g. keto/enol, amide/imidic acid
  • the invention relates to the individual tautomers in isolation, and to mixtures of the tautomers in all proportions.
  • R 1a , R 1b , R 1c and R 1d each independently represent hydrogen or an optionally substituted C 1 -C 6 alkyl, or R 1a is linked to R 1b to form an optionally substituted cycloalkyl ring, or R 1d is linked to R 1c or R 1e to form an optionally substituted cycloalkyl ring;
  • R 1e and R 1f each independently represent hydrogen, fluorine, cyano, hydroxyl, amino, optionally substituted C 1 -C 6 alkyl, optionally substituted C 1 -C 6 alkoxy or an optionally substituted 5 or 6 membered ring, or R 1e and R 1f together form an optionally substituted cycloalkyl ring, or R 1e is linked to R 1d to form an optionally substituted cycloalkyl ring;
  • A is an optionally substituted 5 to 10 membered heteroaryl or aryl ring.
  • the compounds described herein may contain one or more isotopic substitutions, and a reference to a particular element includes within its scope all isotopes of the element.
  • a reference to hydrogen includes within its scope 1 H, 2 H (D), and 3 H (T).
  • references to carbon and oxygen include within their scope respectively 12 C, 13 C and 14 C and 16 O and 18 O.
  • isotopes include 2 H, 3 H, 11 C, 13 C, 14 C, 36 C, 18 F, 123 I, 125 I, 13 N, 15 N, 15 O, 17 O, 18 O, 32 P and 35 S.
  • a reference to a particular functional group also includes within its scope isotopic variations, unless the context indicates otherwise.
  • a reference to an alkyl group such as an ethyl group also covers variations in which one or more of the hydrogen atoms in the group is in the form of a deuterium or tritium isotope, e.g. as in an ethyl group in which all five hydrogen atoms are in the deuterium isotopic form (a perdeuteroethyl group).
  • the isotopes may be radioactive or non-radioactive.
  • the compounds contain no radioactive isotopes. Such compounds are preferred for therapeutic use.
  • the compounds may contain one or more radioisotopes. Compounds containing such radioisotopes may be useful in a diagnostic context.
  • Certain isotopically labelled compounds of formula (I), for example, those incorporating a radioactive isotope, are useful in drug and/or substrate tissue distribution studies.
  • the radioactive isotopes i.e. 3 H and 14 C are particularly useful for this purpose in view of their ease of incorporation and ready means of detection.
  • Substitution with heavier isotopes i.e. 2 H may afford certain therapeutic advantages resulting from greater metabolic stability, for example, increased in vivo half-life or reduced dosage requirements, and hence may be preferred in some circumstances.
  • Substitution with positron emitting isotopes, such as 11 C, 18 F, 15 O and 13 N can be useful in Positron Emission Topography (PET) studies for examining receptor occupancy.
  • PET Positron Emission Topography
  • Isotopically labelled compounds of formula (I) can generally be prepared by conventional techniques known to those skilled in the art or by processes analogous to those described in the accompanying examples and preparations using an appropriate isotopically labelled reagent in place of the non-labelled reagent previously employed.
  • the compounds of formula (I) may exist in crystalline or amorphous form and some of the crystalline forms may exist as polymorphs, which are included within the scope of the present invention.
  • Polymorphic forms of compounds of formula (I) may be characterised and differentiated using a number of conventional analytical techniques, including, but not limited to, infra-red spectra, Raman spectra, X-ray powder diffraction, differential scanning calorimetry, thermogravimetric analysis and solid state nuclear magnetic resonance.
  • the invention provides a compound according to any described embodiments in a crystalline form.
  • the compound may be from 50% to 100% crystalline, and more particularly is at least 50% crystalline, or at least 60% crystalline, or at least 70% crystalline, or at least 80% crystalline, or at least 90% crystalline, or at least 95% crystalline, or at least 98% crystalline, or at least 99% crystalline, or at least 99.5% crystalline, or at least 99.9% crystalline, for example 100% crystalline.
  • the compound may alternatively be in an amorphous form.
  • the invention described herein relates to all crystal forms, solvates and hydrates of any of the disclosed compounds however so prepared. To the extent that any of the compounds disclosed herein have acid or basic centres such as carboxylates or amino groups, then all salt forms of said compounds are included herein. In the case of pharmaceutical uses, the salt should be seen as being a pharmaceutically acceptable salt.
  • the invention relates to any solvates of the compounds and their salts.
  • Preferred solvates are solvates formed by the incorporation into the solid state structure (e.g. crystal structure) of the compounds of the invention of molecules of a non-toxic pharmaceutically acceptable solvent (referred to below as the solvating solvent).
  • solvents include water, alcohols (such as ethanol, isopropanol and butanol) and dimethylsulfoxide.
  • Solvates can be prepared by recrystallising the compounds of the invention with a solvent or mixture of solvents containing the solvating solvent.
  • Whether or not a solvate has been formed in any given instance can be determined by subjecting crystals of the compound to analysis using well known and standard techniques such as thermogravimetric analysis (TGE), differential scanning calorimetry (DSC) and X-ray crystallography.
  • TGE thermogravimetric analysis
  • DSC differential scanning calorimetry
  • X-ray crystallography X-ray crystallography
  • the solvates can be stoichiometric or non-stoichiometric solvates.
  • Particular solvates may be hydrates, and examples of hydrates include hemihydrates, monohydrates and dihydrates.
  • solvates and the methods used to make and characterise them see Bryn et al., Solid-State Chemistry of Drugs, Second Edition, published by SSCI, Inc of West Lafayette, Ind., USA, 1999, ISBN 0-967-06710-3.
  • the invention relates to pharmaceutically functional derivatives of compounds as defined herein including ester derivatives and/or derivatives that have, or provide for, the same biological function and/or activity as any relevant compound of the invention.
  • ester derivatives and/or derivatives that have, or provide for, the same biological function and/or activity as any relevant compound of the invention.
  • prodrugs of compounds as defined herein also includes prodrugs of compounds as defined herein.
  • prodrug of a relevant compound includes any compound that, following oral or parenteral administration, is metabolised in vivo to form that compound in an experimentally-detectable amount, and within a predetermined time (e.g. within a dosing interval of between 6 and 24 hours (i.e. once to four times daily).
  • Prodrugs of compounds may be prepared by modifying functional groups present on the compound in such a way that the modifications are cleaved, in vivo when such prodrug is administered to a mammalian subject. The modifications typically are achieved by synthesizing the parent compound with a prodrug substituent.
  • Prodrugs include compounds wherein a hydroxyl, amino, sulfhydryl, carboxyl or carbonyl group in a compound is bonded to any group that may be cleaved in vivo to regenerate the free hydroxyl, amino, sulfhydryl, carboxyl or carbonyl group, respectively.
  • prodrugs include, but are not limited to, esters and carbamates of hydroxyl functional groups, ester groups of carboxyl functional groups, N-acyl derivatives and N-Mannich bases. General information on prodrugs may be found e.g. in Bundegaard, H. “Design of Prodrugs” p. 1-92, Elsevier, New York-Oxford (1985).
  • Metabolites of compounds of formula (I) are also within the scope of the present invention.
  • the term ‘metabolites’ refers to all molecules derived from any of the compounds according to the present invention in a cell or organism, preferably mammal. Preferably the term relates to molecules which differ from any molecule which is present in any such cell or organism under physiological conditions.
  • a treatment defined herein may be applied as a sole therapy of may involve, in addition to the compounds of the invention, conventional surgery or radiotherapy or chemotherapy.
  • compounds of formula (I) can also be used in combination with existing therapeutic agents for the treatment of conditions associated with cancer, including small molecule therapeutics or antibody based therapeutics.
  • the compounds described herein are characterised by a cyanopyrrolidine core with an amide group and fluorine attached to the same position on the cyannopyrrolidine ring, wherein the amide group is substituted with an optionally substituted aryl or heteroaryl ring.
  • R 1a , R 1b , R 1c and R 1d each independently represent hydrogen or an optionally substituted C 1 -C 6 alkyl, or R 1a is linked to R 1b to form an optionally substituted C 3 -C 6 cycloalkyl ring, or R 1d is linked to R 1c or R 1e to form an optionally substituted C 3 -C 6 cycloalkyl ring;
  • R 1e and R 1f each independently represent hydrogen, fluorine, cyano, hydroxyl, amino, optionally substituted C 1 -C 6 alkyl, optionally substituted C 1 -C 6 alkoxy or an optionally substituted 5 or 6 membered heteroaryl or aryl ring, or R 1e and R 1f together form an optionally substituted C 3 -C 6 cycloalkyl ring, or R 1e is linked to R 1d to form an optionally substituted C 3 -C 6 cycloalkyl ring;
  • A is an optionally substituted monocyclic or bicyclic 5 to 10 membered heteroaryl or aryl ring.
  • R 1a , R 1b , R 1c , Rid may each independently represent hydrogen or optionally substituted C 1 -C 6 alkyl.
  • R 1a , R 1b , R 1c , R 1d may each independently represent hydrogen or C 1 -C 3 alkyl (e.g. methyl or ethyl).
  • R 1a may be hydrogen or C 1 -C 3 alkyl and R 1b may be hydrogen.
  • R 1c may be hydrogen or C 1 -C 3 alkyl and R 1d may be hydrogen.
  • the alkyl may be unsubstituted or substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF 5 .
  • R 1a R 1b , R 1c , Rid each represent hydrogen.
  • R 1a may represent hydrogen.
  • R 1a may represent C 1 -C 6 alkyl.
  • R 1a may represent C 1 -C 3 alkyl, for example, methyl or ethyl.
  • R 1b , R 1c , R 1d , R 1e and R 1f may each represent hydrogen.
  • the alkyl may be unsubstituted or substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF 5 , in particular fluorine.
  • R 1b may represent hydrogen.
  • R 1b may represent C 1 -C 6 alkyl.
  • R 1b may represent C 1 -C 3 alkyl, for example, methyl or ethyl.
  • R 1a , R 1c , R 1d , R 1e and R 1f may each represent hydrogen.
  • the alkyl may be unsubstituted or substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF 5 , in particular fluorine.
  • R 1c may represent hydrogen.
  • R 1c may represent C 1 -C 6 alkyl.
  • R 1c may represent C 1 -C 3 alkyl, for example, methyl or ethyl.
  • R 1a , R 1b , R 1d , R 1e and R 1f may each represent hydrogen.
  • the alkyl may be unsubstituted or substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF 5 , in particular fluorine.
  • R 1d may represent hydrogen.
  • R 1d may represent C 1 -C 6 alkyl.
  • R 1d may represent C 1 -C 3 alkyl, for example, methyl or ethyl.
  • R 1a , R 1b , R 1c , R 1e and R 1f may each represent hydrogen.
  • the alkyl may be unsubstituted or substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF 5 , in particular fluorine.
  • R 1a and R 1b may together form a cycloalkyl ring.
  • R 1c and R 1d may together form a cycloalkyl ring.
  • the cycloalkyl ring can contain 3, 4, 5 or 6 atoms, in particular 3 or 4 atoms.
  • R 1b and R 1c together form a C 3 -C 6 cycloalkyl ring
  • R 1a , R 1d , R 1e and R 1f may be hydrogen.
  • R 1d and R 1e together form a cycloalkyl ring R 1a , R 1b , R 1c and R 1f may each be hydrogen.
  • R 1e may represent hydrogen, fluorine, cyano, hydroxyl, amino, optionally substituted C 1 -C 6 alkyl, optionally substituted C 1 -C 6 alkoxy or an optionally substituted 5 or 6 membered heteroaryl or aryl ring.
  • the alkyl and alkoxy may be substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF 5 .
  • the heteroaryl or aryl ring may be unsubstituted or substituted with halogen, cyano, oxo, nitro, amino, hydroxy, C 1 -C 6 alkyl or C 1 -C 6 alkoxy.
  • R 1e can represent hydrogen, fluorine, C 1 -C 3 alkyl or substituted C 1 -C 3 alkoxy.
  • R 1e can represent fluorine.
  • R 1e can represent methyl.
  • R 1e can represent methoxy.
  • R 1e can represent CF 3 .
  • R 1e can represent OCF 3 .
  • R 1e represents fluorine, cyano, hydroxyl, amino, optionally substituted C 1 -C 6 alkyl, optionally substituted C 1 -C 6 alkoxy or an optionally substituted 5 or 6 membered heteroaryl or aryl ring
  • R 1a , R 1b , R 1c , R 1d and R 1f may each represent hydrogen.
  • R 1e represents hydrogen.
  • R 1f may represent hydrogen fluorine, cyano, hydroxyl, amino, optionally substituted C 1 -C 6 alkyl, optionally substituted C 1 -C 6 alkoxy, or an optionally substituted 5 or 6 membered heteroaryl or aryl ring.
  • the alkyl and alkoxy may be substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF 5 .
  • the heteroaryl or aryl ring may be unsubstituted or substituted with halogen, cyano, oxo, nitro, amino, hydroxy, C 1 -C 6 alkyl or C 1 -C 6 alkoxy.
  • R 1f can represent hydrogen fluorine, unsubstituted or substituted C 1 -C 3 alkyl or unsubstituted or substituted C 1 -C 3 alkoxy.
  • R 1f can represent fluorine.
  • R 1f can represent methyl.
  • R 1f can represent methoxy.
  • R 1f can represent CF 3 .
  • R 1f can represent OCF 3 .
  • R 1f represents fluorine, cyano, hydroxyl, amino, optionally substituted C 1 -C 6 alkyl or optionally substituted C 1 -C 6 alkoxy or an optionally substituted 5 or 6 membered heteroaryl or aryl ring
  • R 1a , R 1b , R 1c , R 1d and R 1e may each represent hydrogen.
  • R 1f represents hydrogen.
  • R 1e and R 1f may together form a cycloalkyl ring.
  • R 1e and R 1d may together form a cycloalkyl ring.
  • the cycloalkyl ring can contain 3, 4, 5 or 6 atoms, in particular 3 or 4 atoms.
  • R 1a , R 1b , R 1c and R 1d may be hydrogen.
  • R 1e and R 1d together form a cycloalkyl ring R 1a , R 1b , R 1c and R 1f may each be hydrogen.
  • the cycloalkyl rings within the definitions of R 1a , R 1b , R 1c , R 1d , R 1e and R 1f may be unsubstituted or substituted with one or more substituents selected from halogen, cyano, oxo, nitro, amino, hydroxy, C 1 -C 3 alkyl, C 1 -C 3 alkoxy, C 1-3 alkylamino, C 2-6 alkenylamino, C 1 -C 3 acylamino, carboxy, C 1 -C 3 alkoxycarbonyl, carboxamidyl, carbamoyl, wherein any hydrocarbyl moiety may itself be substituted by one or more halogen, in particular fluorine.
  • the cycloalkyl ring may be unsubstituted or substituted with one or two substituents selected from halogen, cyano, oxo, nitro, amino, hydroxy, C 1 -C 3 alkyl and C 1 -C 3 alkoxy, wherein the alkyl and alkoxy may be substituted with one or more halogen, in particular fluorine.
  • R 1a , R 1b , R 1c , R 1d , R 1e and R 1f may be other than hydrogen, and the remaining are each hydrogen.
  • R 1a , R 1b , R 1c , R 1d , R 1e and R 1f may be other than hydrogen, and the remaining are each hydrogen.
  • R 1a , R 1b , R 1c , R 1d , R 1e and R 1f may be other than hydrogen, and the remaining are each hydrogen.
  • R 1a , R 1b , R 1c , R 1d , R 1e and R 1f may be other than hydrogen, and the remaining are each hydrogen.
  • R 1a , R 1b , R 1c , R 1d , R 1e and R 1f may be other than hydrogen, and the remaining are each hydrogen.
  • R 1a , R 1b , R 1c , R 1d , R 1e and R 1f may be other than hydrogen, and the remaining are each hydrogen.
  • R 1a , R 1b , R 1c , R 1d , R 1e and R 1f When one, two, three, four, five or six of R 1a , R 1b , R 1c , R 1d , R 1e and R 1f are other than hydrogen, the remaining R groups represent a group in accordance with the definitions above.
  • one, two, three or four of R 1a , R 1b , R 1c , R 1d , R 1e and R 1f may be other than hydrogen and the remaining each represent hydrogen.
  • R 1a , R 1b , R 1c , R 1d , R 1e and R 1f may be other than hydrogen and the remaining each represent hydrogen.
  • the compounds may be in the form where R 1a , R 1b , R 1c , R 1d , R 1e and R 1f are each hydrogen. In such cases the compounds may be of formula (IA):
  • A is an optionally substituted 5 to 10 membered heteroaryl or aryl ring.
  • the heteroaryl or aryl ring of ring A may be defined according to the definition of heteroaryl and aryl ring found herein and may be monocyclic or bicyclic. Where the ring is bicyclic, the second ring may be aromatic, or may be partly saturated, and thus not every atom in the 5 to 10 membered ring need be in an aryl system, there must be at least one aryl or heteroaryl ring within the 5 to 10 atoms, and it is this ring that is attached to the amide nitrogen.
  • A represents a 5 to 10 membered (e.g. 5, 6, 7, 8, 9 or 10 membered) monocyclic or fused bicyclic heteroaryl or aryl ring which may be optionally substituted with one or more (e.g. one, two, three or four) of -Q 1 -(R 2 ) n , in particular one or two of -Q 1 -(R 2 ) n .
  • A may represent a 5 or 6 membered heteroaryl or aryl ring which may be optionally substituted with one or more (e.g. one, two, three or four) of -Q 1 (R 2 ) n .
  • A may represent a 9 or 10 membered bicyclic heteroaryl or aryl ring which may be optionally substituted with one or more (e.g. one, two, three or four) of -Q 1 (R 2 ) n .
  • the ring may be monocyclic or bicyclic and comprise one or more (e.g. 1, 2 or 3) heteroatoms independently selected from nitrogen, oxygen and sulphur.
  • the heteroaryl ring may contain at least one nitrogen atom, for example, 1, 2 or 3 nitrogen atoms, preferably 1 or 2 nitrogen heteroatoms.
  • nitrogen containing heteroaryl rings include pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, pyrrolyl, oxazolyl, thiazolyl, pyrazolyl, triazolyl, tetrazolyl, indolyl, indolizinyl, isoindolyl, indolinyl, purinyl, furazanyl, imidazolyl, indazolyl, isothiazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, thiadiazolyl, benzimidazolyl, benzothiazolyl, napthyridinyl, pteridinyl, pyrazinyl, 4H-quinolizinyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl, imidazopyridin
  • nitrogen containing heteroaryl rings include pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, pyrrolyl, oxazolyl, thiazolyl, pyrazolyl, triazolyl, tetrazolyl, indolyl, indolizinyl, isoindolyl, indolinyl, purinyl, furazanyl, imidazolyl, indazolyl, isothiazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, thiadiazolyl, benzimidazolyl, benzothiazolyl, napthyridinyl, pteridinyl, pyrazinyl, 4H-quinolizinyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl, imidazopyri
  • the optionally substituted 5 to 10 membered heteroaryl or aryl ring may be selected from pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, furyl, pyrrolyl, oxazolyl, thiazolyl, pyrazolyl, triazolyl, tetrazolyl, indolyl, indolizinyl, isoindolyl, purinyl, furazanyl, imidazolyl, indazolyl, isothiazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, thiadiazolyl, benzofuranyl, isobenzofuranyl, benzothiophenyl, isobenzothiophenyl, benzimidazolyl, benzothiazolyl, napthyridinyl, pteridinyl, pyrazinyl, quinolinyl, iso
  • the optionally substituted 5 to 10 membered heteroaryl or aryl ring may be selected from pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, furyl, pyrrolyl, oxazolyl, thiazolyl, pyrazolyl, triazolyl, tetrazolyl, indolyl, indolizinyl, isoindolyl, purinyl, furazanyl, imidazolyl, indazolyl, isothiazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, thiadiazolyl, benzofuranyl, isobenzofuranyl, benzothiophenyl, isobenzothiophenyl, benzimidazolyl, benzothiazolyl, napthyridinyl, pteridinyl, pyrazinyl, quinolinyl,
  • ring A is a fused bicyclic ring where one of the rings is aromatic and the other is at least partially saturated, attachment to the cyanopyrrolidine ring via the amide is from the aromatic ring of the bicycle.
  • ring A is selected from thiazolyl, imidazolyl, isoxazolyl, pyrazolyl, phenyl, benzothiazolyl, imidazopyridinyl and quinolinyl.
  • ring A may be unsubstituted or substituted with one or more -Q 1 -(R 2 ) wherein each occurrence of -Q 1 -(R 2 ) n is the same or different, and wherein:
  • n 0 or 1
  • Q 1 represents halogen, cyano, oxo, nitro, —OR 3 , —SR 3 , —NR 3 R 4 , —CONR 3 R 4 , —NR 3 COR 4 , —NR 3 CONR 4 R 5 , —COR 3 , —C(O)OR 3 , —SO 2 R 3 , —SO 2 NR 3 R 4 , —NR 3 SO 2 R 4 , —NR 3 SO 2 NR 4 R 5 , —NR 3 C(O)OR 4 , optionally substituted —C 1 -C 6 alkyl, optionally substituted —C 1 -C 6 alkoxy, optionally substituted —C 2 -C 6 alkenyl, optionally substituted —C 2 -C 6 alkynyl, a covalent bond, an oxygen atom, a sulphur atom, —SO—, —SO 2 —, —CO—, —C(O)O—, —
  • R 3 , R 4 and R 5 each independently represent hydrogen, optionally substituted C 1 -C 6 alkyl or optionally substituted C 1 -C 6 alkylene.
  • R 2 represents an optionally substituted 3 to 10 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring (when n is 0, Q 1 is present and R 2 is absent).
  • Ring A may be unsubstituted or substituted with one, two, three or four of -Q 1 -(R 2 ) n .
  • ring A is either unsubstituted or substituted with one or two of -Q 1 -(R 2 ) n .
  • Each occurrence of -Q 1 -(R 2 ) n may be the same or different.
  • ring A may be either unsubstituted or substituted with one of -Q 1 -(R 2 ) n .
  • Q 1 , R 2 and n are as defined herein.
  • Q 1 may be selected from halogen (e.g. fluorine, chlorine or bromine), cyano, oxo, nitro, —OR 3 (e.g hydroxyl), —SR 3 (e.g. thiol), —NR 3 R 4 (e.g. amino or N,N-dimethylamino), —CONR 3 R 4 (e.g. amido), —NR 3 COR 4 (N-acetyl), —NR 3 CONR 4 R 5 , —COR 3 (e.g. acetyl), —C(O)OR 3 (e.g. methoxycarbonyl or ethoxycarbonyl), —SO 2 R 3 (e.g.
  • methyl sulphonyl methyl sulphonyl
  • SO 2 NR 3 R 4 e.g. dimethylaminosulphonyl
  • —NR 3 SO 2 R 4 e.g. dimethylaminosulphonyl
  • —NR 3 SO 2 R 4 e.g. dimethylaminosulphonyl
  • —NR 3 SO 2 R 4 e.g. dimethylaminosulphonyl
  • —NR 3 SO 2 R 4 e.g. dimethylaminosulphonyl
  • —NR 3 SO 2 R 4 e.g. dimethylaminosulphonyl
  • —NR 3 SO 2 R 4 e.g. dimethylaminosulphonyl
  • —NR 3 SO 2 R 4 e.g. dimethylaminosulphonyl
  • —NR 3 SO 2 R 4 e.g. dimethylaminosulphonyl
  • —NR 3 SO 2 R 4 e.g. dimethylaminosulphonyl
  • C 1 -C 4 alkylene e.g. methylene or ethylene
  • optionally substituted —C 2 -C 4 alkenylene e.g. vinyl
  • ring A may be substituted with one or more (e.g. one, two, three or four) Q 1 substituents independently selected from halogen (e.g. fluorine, chlorine or bromine), cyano, oxo, nitro, —OR 3 , —SR 3 , —NR 3 R 4 , —CONR 3 R 4 , —NR 3 C(O)R 4 , —NR 3 C(O)NR 4 R 5 , —C(O)R 3 , —C(O)OR 3 , —SO 2 R 3 , —SO 2 NR 3 R 4 , —NR 3 SO 2 R 4 , —NR 3 SO 2 NR 4 R 5 , —NR 3 C(O)OR 4 , —C 1 -C 6 alkyl, —C 1 -C 6 alkoxy, —C 2 -C 6 alkenyl, or —C 2 -C 6 alkynyl, wherein alkyl, alk
  • Q 1 may represent halogen (e.g. fluorine or chlorine), C 1 -C 6 alkyl or C 1 -C 3 alkyl optionally substituted with one or more fluorine, e.g. CF 3 .
  • halogen e.g. fluorine or chlorine
  • C 1 -C 6 alkyl or C 1 -C 3 alkyl optionally substituted with one or more fluorine, e.g. CF 3 .
  • n is 0 and ring A represents a 5 or 6 membered heteroaryl or aryl ring which is optionally substituted with one or more (e.g. one, two, three or four) Q 1 substituents independently selected from halogen (e.g. fluorine or chlorine), C 1 -C 6 alkyl or C 1 -C 3 alkyl optionally substituted with one or more fluorine, e.g. CF 3 .
  • halogen e.g. fluorine or chlorine
  • C 1 -C 6 alkyl or C 1 -C 3 alkyl optionally substituted with one or more fluorine, e.g. CF 3 .
  • n is 0 and ring A represents a 9 or 10 membered heteroaryl or aryl ring which is optionally substituted with one or more (e.g. one, two, three or four) Q 1 substituents independently selected from halogen (e.g. fluorine or chlorine), C 1 -C 6 alkyl or C 1 -C 3 alkyl optionally substituted with one or more fluorine, e.g. CF 3 .
  • halogen e.g. fluorine or chlorine
  • C 1 -C 6 alkyl or C 1 -C 3 alkyl optionally substituted with one or more fluorine, e.g. CF 3 .
  • Q 1 is a covalent bond or a linker selected from covalent bond, an oxygen atom, a sulphur atom, —SO—, —SO 2 —, —CO—, —C(O)O—, —CONR 3 —, —NR 3 —, —NR 3 CO—, —NR 3 CONR 4 —, —SO 2 NR 3 —, —NR 3 SO 2 —, —NR 3 SO 2 NR 4 —, —NR 3 C(O)O—, —NR 3 C(O)OR 4 —, C 1 -C 6 alkylene or —C 2 -C 6 alkenylene, wherein the alkylene or alkenylene is optionally substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF 5 .
  • Q 1 is a covalent bond, an oxygen atom, C 1 -C 6 alkylene or C 1 -C 3 alkylene, wherein the alkylene is optionally substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF 5 .
  • ring A is substituted with a further ring either directly or via a linker, i.e. ring A is substituted with at least one -Q 1 -(R 2 ) n wherein n is 1. Substitution with a further ring is especially preferred when ring A is a monocycle.
  • R 2 represents a 3 to 10 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring.
  • R 2 may be selected from cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, decahydronaphthalenyl, phenyl, naphthyl, naphthalenyl, pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, furyl, pyrrolyl, oxazolyl, thiazolyl, pyrazolyl, tetrazolyl, indolyl, indolizinyl, isoindolyl, indolinyl, purinyl, furazanyl, imidazolyl, indazolyl, isothiazolyl, isoxazolyl, oxadia
  • R 2 may be selected from cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, decahydronaphthalenyl, phenyl, naphthyl, naphthalenyl, pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, furyl, pyrrolyl, oxazolyl, thiazolyl, pyrazolyl, tetrazolyl, indolyl, indolizinyl, isoindolyl, indolinyl, purinyl, furazanyl, imidazolyl, indazolyl, isothiazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, thiadiazolyl, benzofuranyl, isobenzofuranyl, benzothioph
  • R 2 may represent an optionally substituted 5 or 6 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring.
  • R 2 may represent an optionally substituted 9 or 10 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring.
  • R 2 is selected from substituted or unsubstituted phenyl, pyrazolyl, indazolyl, imidazolyl and thiazolyl. More particularly, R 2 is phenyl.
  • R 2 may be optionally substituted with one or more substituents selected from halogen, cyano, oxo, nitro, —OR 6 , —SR 6 , —NR 6 R 7 , —CONR 6 R 7 , —NR 6 COR 7 , —NR 6 CONR 7 R 8 , —COR 6 , —C(O)OR 6 , —SO 2 R 6 , —SO 2 NR 6 R 7 , —NR 6 SO 2 R 7 , —NR 6 SO 2 NR 7 R 8 , —NR 6 C(O)OR 7 , optionally substituted —C 1 -C 6 alkyl, optionally substituted —C 1 -C 6 alkoxy, optionally substituted —C 2 -C 6 alkenyl, optionally substituted —C 2 -C 6 alkynyl, -Q 2 -R 6 , -Q 2 -NR 6 CONR 7 R 8 , -Q
  • Q 2 represents a covalent bond, an oxygen atom, a sulphur atom, —SO—, —SO 2 —, —CO—, optionally substituted C 1 -C 6 alkylene or optionally substituted C 2 -C 6 alkenylene;
  • R 6 , R 7 , R 8 each independently represent hydrogen, optionally substituted C 1 -C 6 alkyl, optionally substituted heterocyclyl, optionally substituted heteroaryl, optionally substituted aryl, or an optionally substituted cycloalkyl.
  • R 2 may be substituted with one or more (e.g. one, two, three or four), in particular one or two, substituents independently selected from halogen, cyano, oxo, nitro, —OR 6 , —SR 6 , —NR 6 R 7 , —CONR 6 R 7 , —NR 6 COR 7 , —NR 6 CONR 7 R 8 , —COR 6 , —C(O)OR 6 , —SO 2 R 6 , —SO 2 NR 6 R 7 , —NR 6 SO 2 R 7 , —NR 6 SO 2 NR 7 R 8 , —NR 6 C(O)OR 7 , optionally substituted —C 1 -C 6 alkyl, optionally substituted —C 1 -C 6 alkoxy, optionally substituted —C 2 -C 6 alkenyl, optionally substituted —C 2 -C 6 alkynyl, -Q 2 -R 6 , -Q 2 -
  • R 2 may be substituted with one or more substituents selected from cyano, C(O)NR 6 R 7 , —C 1 -C 4 alkyl (e.g. propyl, isobutyl or tert butyl) or C 1 -C 2 alkyl (e.g. methyl or ethyl), and a 3 to 10 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring, wherein R 6 and R 7 each independently represent hydrogen or optionally substituted C 1 -C 6 alkyl.
  • the alkyl may be optionally substituted with one or more fluorine.
  • R 2 may be mono-substituted with a substituent selected from cyano, C(O)NR 6 R 7 , —C 1 -C 3 alkyl, in particular methyl, and imidazolyl, wherein R 6 and R 7 each independently represent hydrogen or methyl.
  • R 2 may be optionally substituted with a further optionally substituted 3 to 10 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring, either directly attached or via a linking group.
  • the linking group may be an oxygen atom, a carbonyl or an optionally substituted C 1 -C 6 alkylene.
  • the linking group may be oxygen, —CO— or an alkylene chain, for example, methylene.
  • the 3 to 10 membered ring may be unsubstituted or substituted with one or more (e.g. one, two, three of four), in particular one or two, substituents selected from halogen (for example, fluorine or chlorine), C 1 -C 4 alkyl (e.g.
  • propyl isobutyl or tert butyl
  • C 1 -C 2 alkyl e.g. methyl or ethyl
  • the alkyl may be optionally substituted with one or more fluorine.
  • the 3 to 10 membered ring is unsubstituted.
  • R 2 may be unsubstituted, mono-substituted or di-substituted. More particularly, R 2 is unsubstituted or mono-substituted.
  • R 2 represents a 3 to 10 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring selected from heterocyclyl, cycloalkyl, heteroaryl or aryl ring selected from cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, decahydronaphthalenyl, phenyl, naphthyl, naphthalenyl, pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, furyl, pyrrolyl, oxazolyl, thiazolyl, pyrazolyl, tetrazolyl, indolyl, indolizinyl, isoindolyl, indolinyl, purinyl, furazanyl, imidazolyl, indazolyl, isothi
  • R 2 may represent a ring selected from phenyl, pyrazolyl, indazolyl, imidazolyl and thiazolyl, wherein the ring is unsubstituted or substituted with one or more, in particular one or two, substituents selected from halogen (e.g.
  • R 2 may represent a ring selected from cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, decahydronaphthalenyl, phenyl, naphthyl, naphthalenyl, pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, furyl, pyrrolyl, oxazolyl, thiazolyl, pyrazolyl, tetrazolyl, indolyl, indolizinyl, isoindolyl, indolinyl, purinyl, furazanyl, imidazolyl, indazolyl, isothiazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, thiadiazolyl, benzofuranyl, isobenzofuranyl, benzo
  • propyl isobutyl or tert butyl or C 1 -C 2 alkyl (e.g. methyl or ethyl), and a 3 to 10 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring, wherein R 6 and R 7 each independently represent hydrogen or optionally substituted C 1 -C 6 alkyl.
  • the alkyl may be optionally substituted with one or more fluorine.
  • R 2 may be selected from phenyl, pyrazolyl, indazolyl, imidazolyl and thiazolyl wherein the ring is unsubstituted or substituted with one or more (e.g. one, two or three) substitutents selected from cyano, C(O)NR 6 R 7 , —C 1 -C 6 alkyl, and a 3 to 10 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring, wherein R 6 and R 7 each independently represent hydrogen or optionally substituted C 1 -C 6 alkyl.
  • the present invention further relates to compounds of formula (I), or a pharmaceutically acceptable salt thereof, wherein:
  • R 1a , R 1b , R 1e and R 1d each independently represent hydrogen or C 1 -C 3 alkyl which may be optionally substituted with one or more fluorine;
  • R 1e and R 1f independently represent hydrogen, fluorine, C 1 -C 3 alkyl or C 1 -C 3 alkoxy, wherein the alkyl or alkoxy may be optionally substituted with one or more fluorine;
  • A represents a 5 to 10 membered monocyclic or bicyclic heteroaryl or aryl ring which is unsubstituted or substituted with one, two or three of -Q 1 -(R 2 ) n ;
  • n 0 or 1
  • Q 1 , R 2 and n are as defined herein.
  • Q 1 is selected from halogen (e.g. fluorine, chlorine or bromine), cyano, oxo, nitro, —OR 3 (e.g hydroxyl), —SR 3 (e.g. thiol), —NR 3 R 4 (e.g. amino or N,N-dimethylamino), —CONR 3 R 4 (e.g. amido), —NR 3 COR 4 (N-acetyl), —NR 3 CONR 4 R 5 , —COR 3 (e.g. acetyl), —C(O)OR 3 (e.g. methoxycarbonyl or ethoxycarbonyl), —SO 2 R 3 (e.g.
  • methyl sulphonyl methyl sulphonyl
  • SO 2 NR 3 R 4 e.g. dimethylaminosulphonyl
  • —NR 3 SO 2 R 4 e.g. dimethylaminosulphonyl
  • —NR 3 SO 2 R 4 e.g. dimethylaminosulphonyl
  • —NR 3 SO 2 R 4 e.g. dimethylaminosulphonyl
  • —NR 3 SO 2 R 4 e.g. dimethylaminosulphonyl
  • —NR 3 SO 2 R 4 e.g. dimethylaminosulphonyl
  • —NR 3 SO 2 R 4 e.g. dimethylaminosulphonyl
  • —NR 3 SO 2 R 4 e.g. dimethylaminosulphonyl
  • —NR 3 SO 2 R 4 e.g. dimethylaminosulphonyl
  • —NR 3 SO 2 R 4 e.g. dimethylaminosulphonyl
  • R 2 is a 5 or 6 membered heteroaryl, heterocyclyl or aryl ring optionally substituted with one or two substituents independently selected from halogen, cyano, oxo, nitro, —OR 6 , —SR 6 , —NR 6 R 7 , —CONR 6 R 7 , —NR 6 COR 7 , —NR 6 CONR 7 R 8 , —COR 6 , —C(O)OR 6 , —SO 2 R 6 , —SO 2 NR 6 R 7 , —NR 6 SO 2 R 7 , —NR 6 SO 2 NR 7 R 8 , —NR 6 C(O)OR 7 , optionally substituted —C 1 -C 6 alkyl, optionally substituted —C 1 -C 6 alkoxy, optionally substituted —C 2 -C 6 alkenyl, optionally substituted —C 2 -C 6 alkynyl, -Q 2 -R 6 ,
  • the present invention further relates to compounds of formula (I), or a pharmaceutically acceptable salt thereof, wherein:
  • R 1a , R 1b , R 1c and R 1d are each hydrogen;
  • A represents a 5 to 10 membered monocyclic or bicyclic heteroaryl or aryl ring which is unsubstituted or substituted with one or two of -Q 1 -(R 2 ) n ;
  • Q 1 represents halogen (e.g. fluorine or chlorine), C 1 -C 6 alkyl or C 1 -C 3 alkyl optionally substituted with one or more fluorine, a covalent bond, an oxygen atom, C 1 -C 6 alkylene or C 1 -C 3 alkylene, wherein the alkylene is optionally substituted with one or more substitutents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF 5 ;
  • halogen e.g. fluorine or chlorine
  • C 1 -C 6 alkyl or C 1 -C 3 alkyl optionally substituted with one or more fluorine, a covalent bond, an oxygen atom, C 1 -C 6 alkylene or C 1 -C 3 alkylene, wherein the alkylene is optionally substituted with one or more substitutents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF 5 ;
  • R 2 represents a 5 to 10 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring, in particular, R 2 represents phenyl, pyrazolyl, indazolyl, imidazolyl and thiazolyl.
  • heteroaryl and aryl ring represented by A examples include those shown below:
  • ring A represents the point of attachment to the remainder of the molecule, i.e. to the amide nitrogen, and wherein ring A is optionally substituted with one or more of -Q 1 -(R 2 ) n .
  • Hydrogen atoms attached to the ring nitrogen atoms have not been shown. It will be understood by the skilled person which ring nitrogen atoms are suitable for substitution and where not substituted the nitrogen may be bound to a hydrogen atom to complete its valency, where appropriate.
  • novel compounds of formula (I) include:
  • a process for the preparation of a compound of formula (I) or a pharmaceutically acceptable salt thereof comprising the steps of reacting an acid of formula (III) with a compound A-NH 2 to form an amide:
  • R 1a -R 1f are as defined elsewhere and PG is an amine protecting group.
  • the protecting group may be but is not limited to BOC. It is clear to a person skilled in the art to combine or adjust such a protecting chemical group. After coupling of A-NH 2 to form an amide, the protecting group may be removed to leave the free amine according to formula (IV) which can then be treated with cyanogen bromide to form compounds according to formula (I).
  • R 1a -R 1f and A are as defined elsewhere.
  • composition comprising a compound of the invention.
  • compositions of this invention comprise any of the compounds of the invention combined with any pharmaceutically acceptable carrier, adjuvant or vehicle.
  • compositions may be in the form of, for example, tablets, capsules, powders, granules, elixirs, lozenges, suppositories, syrups and liquid preparations including suspensions and solutions.
  • pharmaceutical composition in the context of this invention means a composition comprising an active agent and comprising additionally one or more pharmaceutically acceptable carriers.
  • composition may further contain ingredients selected from, for example, diluents, adjuvants, excipients, vehicles, preserving agents, fillers, disintegrating agents, wetting agents, emulsifying agents, suspending agents, sweetening agents, flavouring agents, perfuming agents, antibacterial agents, antifungal agents, lubricating agents and dispersing agents, depending on the nature of the mode of administration and dosage forms.
  • ingredients selected from, for example, diluents, adjuvants, excipients, vehicles, preserving agents, fillers, disintegrating agents, wetting agents, emulsifying agents, suspending agents, sweetening agents, flavouring agents, perfuming agents, antibacterial agents, antifungal agents, lubricating agents and dispersing agents, depending on the nature of the mode of administration and dosage forms.
  • the compounds of the invention may be used in the treatment of disorders and diseases related to DUB inhibition, particularly Cezanne 1 and USP30 inhibition.
  • a compound of formula (I) or pharmaceutical composition thereof for use in therapy there is provided a compound of formula (I) or pharmaceutical composition thereof for use in therapy.
  • the compounds of the invention have use in the treatment of cancer and more particularly in the treatment of cancers linked to DUB activity.
  • Compounds of the invention may be useful against any DUB enzyme, including but not limited to Cezanne 1 and USP30.
  • the compounds described herein may be used in the manufacture of a medicament for the treatment of cancer linked to DUB activity.
  • a method of treatment or prevention of cancer linked to Cezanne 1 or USP30 activity comprising administering a pharmaceutically effective amount of a compound of the invention or a pharmaceutical composition thereof to an individual suffering from a cancer linked to Cezanne 1 or USP30 activity.
  • cancer or “tumour” include but are not limited to breast, ovarian, prostate, lung, kidney, gastric, colon, testicular, head and neck, pancreas, brain, melanoma, bone or other cancers of tissue organs and cancers of the blood cells such as lymphomas and leukaemias.
  • cancers include lymphoma, multiple myeloma, colorectal cancer, and non-small cell lung carcinoma.
  • the compounds or compositions disclosed herein may be used to treat additional diseases linked to Cezanne 1 activity.
  • the compounds of the invention or pharmaceutical compositions thereof as described herein may be combined with one or more additional agents.
  • the compounds may be combined with one or more additional anti-tumour therapeutic agents, for example chemotherapeutic drugs or inhibitors of other regulatory proteins.
  • the one or more anti-tumour therapeutic agent is selected from a PARP (poly ADP ribose polymerase) inhibitor, a BRCA2 inhibitor and an ATM inhibitor.
  • the PARP (poly ADP ribose polymerase) inhibitor is an inhibitory RNA (RNAi) molecule (PARPi).
  • PARP inhibitors may be selected from one or more of Iniparib (BSI 201), Olaparib (AZD-2281), Rucaparib (AG014699, PF-01367338) and Veliparib (ABT-888), MK-4827, CEP-9722, E7016(GPI-21016), LT-673, MP-124, NMS-P118.
  • the one or more anti-tumour agent is a chemotherapeutic agent.
  • Chemotherapeutic agents may be selected from olaparib, mitomycin C, cisplatin, carboplatin, oxaliplatin, ionizing radiation (IR), camptothecin, irinotecan, topotecan, temozolomide, taxanes, 5-fluoropyrimidines, gemcitabine, and doxorubicin.
  • the compounds of the invention may be useful in the treatment of disorders and diseases related to USP30 inhibition.
  • the compounds of the invention may therefore be useful in the treatment of disorders or diseases having a component relating to mitochondiral dysfunction.
  • Mitochondrial dysfunctions result from defects of the mitochondria, which are specialized compartments present in every cell of the body except red blood cells. When mitochondria fail, less and less energy is generated within the cell and cell injury or even cell death will follow. If this process is repeated throughout the body the life of the subject in whom this is happening is severely compromised. Diseases of the mitochondria appear most often in organs that are very energy demanding such as the brain, heart, liver, skeletal muscles, kidney and the endocrine and respiratory system.
  • the condition involving mitochondrial dysfunction may be selected from a condition involving a mitophagy defect, a condition involving a mutation in mitochondrial DNA, a condition involving mitochondrial oxidative stress, a condition involving a defect in mitochondrial membrane potential, mitochondrial biogenesis, a condition involving a defect in mitochondrial shape or morphology, and a condition involving a lysosomal storage defect.
  • the condition involving mitochondrial dysfunction may be selected from a neurodegenerative disease; multiple sclerosis (MS), mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome; Leber's hereditary optic neuropathy (LHON); cancer; neuropathy, ataxia, retinitis pigmentosa-maternally inherited Leigh syndrome (NARP-MILS); Danon disease; diabetes; diabetic nephropathy; metabolic disorders; heart failure; ischemic heart disease leading to myocardial infarction; psychiatric diseases, for example schizophrenia; multiple sulfatase deficiency (MSD); mucolipidosis II (ML II); mucolipidosis III (ML III); mucolipidosis IV (ML IV); GMl-gangliosidosis (GM1); neuronal ceroid-lipofuscinoses (NCL1); Alpers disease; Barth syndrome; Beta-oxidation defects; carnitine-acyl-carni
  • the condition involving mitochondrial dysfunction may be a CNS disorder, for example a neurodegenerative disease.
  • Neurodegenerative diseases include, but are not limited to, Parkinson's disease, Alzheimer's disease, amyotrophic lateral sclerosis (ALS), Huntington's disease, ischemia, stroke, dementia with Lewy bodies, and frontotemporal dementia.
  • the condition involving mitochondrial dysfunction is a CNS disorder.
  • compositions of the invention may be designed for administration by the oral, parenteral or mucosal route and the choice or the specific form of composition is dependent on the administration route.
  • the composition may be in the form, for example, of tablets, lozenges, dragees, films, powders, elixirs, syrups, liquid preparations including dispersions, suspensions, emulsions, solutions or sprays, cachets, granules, capsules, etc.
  • the composition may be in the form of sprays, inhalants, dispersions, suspensions, emulsions, solutions, gels, patches, films, ointments, creams, lotions, suppositories etc.
  • parenteral administration the composition is in the form of a liquid preparation such as a solution, dispersion, emulsion or suspension including liposome compositions.
  • Preparations according to the invention for parenteral administration include sterile aqueous, aqueous-organic, and organic solutions, suspensions and emulsions.
  • Such dosage forms are prepared according to techniques known in the art of pharmaceutical formulation.
  • the pharmaceutical compositions When in the form of sprays or inhalants the pharmaceutical compositions may be administered nasally. Suitable formulations for this purpose are known to those skilled in the art.
  • compositions of the invention may be administered by injection and may be in the form of a sterile liquid preparation for injection, including liposome preparations.
  • the pharmaceutical compositions of the invention may also be in the form of suppositories for rectal administration.
  • compositions are solid at room temperature and liquid at body temperature to allow release of the active compound.
  • the dosages may be varied depending upon the requirements of the patient, the severity of the condition being treated, and the compound being employed. Determination of the proper dosage for a particular situation is within the remit of the person skilled in the skill of the art. Generally, treatment is initiated with smaller dosages which are less than the optimal dose of the compound. Thereafter the dosage is increased by small increments until the optimum effect under the circumstances is reached.
  • the magnitude of an effective dose of a compound will, of course, vary with the nature of the severity of the condition to be treated and with the particular compound and its route of administration. The selection of appropriate dosages is within the ability of one of ordinary skill in this art, without undue burden.
  • the daily dose range is about 10 ⁇ g to about 100 mg per kg body weight of a human and non-human animal and in general may be around 10 ⁇ g to 30 mg per kg body weight per dose.
  • the above dose may be given from one to three times per day.
  • Compounds of the invention may be prepared via a variety of synthetic routes. Exemplary routes to certain compounds of the invention are shown below. Representative compounds of the present invention can be synthesized in accordance with the general synthetic methods described below and are illustrated more particularly in the schemes that follow. Since the schemes are an illustration, the invention should not be construed as being limited by the chemical reactions and conditions expressed. The preparation of the various starting materials used in the schemes is well within the skill of persons versed in the art. Those skilled in the art appreciate that, where appropriate, the individual transformations within a scheme can be completed in a different order. The following schemes describe general synthetic methods whereby intermediate and target compounds of the present invention may be prepared.
  • Step a To a solution of 4-nitroimidazole (5 g, 44.2 mmol) in MeOH (40 ml) was added phenyl boronic acid (8.77 g, 71.66 mmol) at rt and treated with CuCl 2 (0.71 g, 5.3 mmol) and NaOH (1.76 g, 44.2 mmol). The reaction mixture was stirred at 80° C. for 16 h whilst continuing the slow purging of O 2 gas throughout the reaction time. The resulting reaction mixture was allowed to cool to rt and the purging of O 2 gas was removed. The reaction mixture was then concentrated under reduced pressure. The obtained crude material was poured into water (500 ml) and extracted with EtOAc (3 ⁇ 150 ml).
  • Pd(dppf)Cl 2 (0.074 g, 0.101 mmol) was added to the reaction mixture at rt.
  • the reaction mixture was heated at 105° C. for 1 h.
  • the resulting reaction mixture was allowed to cool at rt, poured into water (20 ml) and extracted with EtOAc (2 ⁇ 20 ml).
  • the combined organic phase was separated, dried over Na 2 SO 4 , filtered and concentrated under reduced pressure.
  • 6-bromoimidazo[1,2-a]pyridin-2-amine and tert-butyl 3-fluoro-3-formylpyrrolidine-1-carboxylate were used in a procedure similar to that described for step a of Example 8 to afford tert-butyl 3-((6-bromoimidazo[1,2-a]pyridin-2-yl)carbamoyl)-3-fluoropyrrolidine-1-carboxylate.
  • tert-butyl 3-((6-bromoimidazo[1,2-a]pyridin-2-yl)carbamoyl)-3-fluoropyrrolidine-1-carboxylate and (1H-pyrazol-5-yl)boronic acid were used in a procedure similar to Example 21 step a to afford tert-butyl 3-((6-(1H-pyrazol-5-yl)imidazo[1,2-a]pyridin-2-yl)carbamoyl)-3-fluoropyrrolidine-1-carboxylate.
  • the Cezanne 1 construct was PCR amplified and cloned into a pFLAG-CMV-6c vector (Sigma-Aldrich) with an N-terminal FLAG tag.
  • HEK293T cells were transfected with FLAG-Cezanne 1 using TransIT-LT1 transfection reagent (Mirus) according to the manufacturer's instructions. Cells were harvested 48 hours after transfection.
  • lysis buffer 50 mM Tris, pH 7.5, 150 mM NaCl, 3 mM EDTA, 0.5% NP40, 10% glycerol, 5 mM beta-mercaptoethanol, protease inhibitors (complete mini, Roche) and phosphatase inhibitors (PhosSTOP mini, Roche). Lysates were incubated for 30 min on ice and centrifuged at 4000 rpm for 10 min at 4° C.
  • Soluble supernatant was added to FLAG affinity resin (EZview Red ANTI-FLAG M2 affinity gel, Sigma-Aldrich) equilibrated in low salt buffer (20 mM Tris, pH 7.5, 150 mM NaCl, 0.5 mM EDTA, 5 mM beta-mercaptoethanol) and incubated at 4° C. for 3 hours rotating. The resin was spun at 2000 rpm for 2 min and the supernatant was removed.
  • FLAG affinity resin EZview Red ANTI-FLAG M2 affinity gel, Sigma-Aldrich
  • the resin was washed two times with low salt buffer and one time with high salt buffer (20 mM Tris, pH 7.5, 500 mM NaCl, 0.5 mM EDTA, 5 mM beta-mercaptoethanol, protease inhibitors (complete mini, Roche) and phosphatase inhibitors (PhosSTOP mini, Roche).
  • elution buffer (10 mM Tris, pH 7.5, 150 mM NaCl, 0.5 mM EDTA, 10% glycerol, 0.5% NP40, 5 mM beta-mercaptoethanol, 0.15 mg/ml 3 ⁇ FLAG peptide (Sigma-Aldrich) was added to the resin and incubated at 4° C. for 2.5 hours while rotating.
  • the resin was centrifuged at 4000 rpm for 30 seconds, and the supernatant containing purified FLAG-Cezanne 1 was removed and stored at ⁇ 80° C.
  • reactions were performed in duplicate in black 384 well plates (small volume, Greiner 784076) in a final reaction volume of 21 ⁇ l.
  • Cezanne 1 was diluted in reaction buffer (40 mM Tris, pH 7.5, 0.005% Tween 20, 0.5 mg/ml BSA, 5 mM—beta-mercaptoethanol) to the equivalent of 0, 0.001, 0.050, 0.01 and 0.05 ⁇ l/well.
  • Buffer was optimised for optimal temperature, pH, reducing agent, salts, time of incubation, and detergent.
  • Reactions were initiated by the addition of 50 nM of TAMRA labelled peptide linked to ubiquitin via an iso-peptide bond as fluorescence polarisation substrate. Reactions were incubated at room temperature and read every 2 min for 120 min. Readings were performed on a Pherastar Plus (BMG Labtech). ⁇ Excitation 540 nm; ⁇ Emission 590 nm.
  • Dilution plates were prepared at 21 times the final concentration (2100 ⁇ M for a final concentration of 100 ⁇ M) in 50% DMSO in a 96-well polypropylene V-bottom plate (Greiner #651201). A typical 8-point dilution series to be 100, 30, 10, 3, 1, 0.3, 0.1, 0.03 M final. Reactions were performed in duplicate in black 384 well plates (small volume, Greiner 784076) in a final reaction volume of 21 ⁇ l. Either 1 ⁇ l of 50% DMSO or diluted compound was added to the plate.
  • Cezanne 1 was diluted in reaction buffer (40 mM Tris, pH 7.5, 0.005% Tween 20, 0.5 mg/ml BSA, 5 mM—beta-mercaptoethanol) to the equivalent of 0.005 ⁇ l/well and 10 ⁇ l of diluted Cezanne 1 was added to the compound. Enzyme and compound were incubated for 30 min at room temp. Reactions were initiated by the addition of 50 nM of TAMRA labelled peptide linked to ubiquitin via an iso-peptide bond as fluorescence polarisation substrate. Reactions were read immediately after addition of substrate and following a 2 hr incubation at room temperature. Readings were performed on a Pherastar Plus (BMG Labtech). ⁇ Excitation 540 nm; ⁇ Emission 590 nm.
  • Example IC50 range 1 C 2 C 3 B 4 C 5 C 6 C 7 C 8 B 9 B 10 B 11 C 12 C 13 A 14 C 15 C 16 C 17 C 18 B 19 B 20 B 21 B 22 B 23 B 24 B 25 B 26 B 27 B 28 B 29 C

Abstract

The present invention relates to novel compounds and methods for the manufacture of inhibitors of deubiquitylating enzymes (DUBs). In particular, the invention relates to the inhibition of Cezanne 1 and ubiquitin C-terminal hydrolase 30 or Ubiquitin Specific Peptidase 30 (USP30). The invention further relates to the use of DUB inhibitors in the treatment of cancer. Compounds of the invention include compounds having the formula (I): pharmaceutically acceptable salt thereof, wherein R1a, R1b, R1c, R1d, R1e, R1f and A are as defined herein.
Figure US20180362460A1-20181220-C00001

Description

  • The present invention relates to novel compounds and methods for the manufacture of inhibitors of deubiquitylating enzymes (DUBs). In particular, the invention relates to the inhibition of Cezanne 1. The invention further relates to the use of DUB inhibitors in the treatment of cancer.
    • BACKGROUND TO THE INVENTION
  • The listing or discussion of an apparently prior-published document in this specification should not necessarily be taken as an acknowledgement that the document is part of the state of the art or is common general knowledge.
  • Ubiquitin is a small protein consisting of 76 amino acids that is important for the regulation of protein function in the cell. Ubiquitylation and deubiquitylation are enzymatically mediated processes by which ubiquitin is covalently bound or cleaved from a target protein. These processes have been implicated in the regulation of many cellular functions including cell cycle progression, apoptosis, modification of cell surface receptors, regulation of DNA transcription and DNA repair. Thus, the ubiquitin system has been implicated in the pathogenesis of numerous disease states including inflammation, viral infection, metabolic dysfunction, CNS disorders, and oncogenesis.
  • Ubiquitin molecules are cleaved from proteins by deubiquitylating enzymes (DUBs), of which there are approximately 95 DUBs in human cells, divided into sub-families based on sequence homology. The ovarian tumour (OTU) family consists of at least 14 active DUBs and are characterised by the presence of an OTU domain and the tendency to cleave ubiquitin chains in a linkage specific manner. Cezanne 1, also known as OTUD7B, is an 843 amino acid protein that was identified owing to its similarity to the OTU family member A20 that has been shown biochemically to have a strong preference for K11 ubiquitin chain linkages.
  • Cezanne 1 has been shown to act as a negative regulator of both the canonical and the non-canonical NF-κB pathway. It has been shown that Cezanne 1 acts on the canonical pathway by processing K63 chains on the RIP 1 protein and on the non-canonical pathway by deubiquitylation of the inhibitory component TRAF3 (TNF receptor associated factor 3). It has also been shown to have a role in hypoxia by regulating HIF1α (hypoxia inducible factor 1α) protein levels. Cezanne 1 siRNA decreased HIF1α protein levels under hypoxia, and accordingly decreased HIF1α target gene expression. Knockdown of Cezanne 1 led to higher levels of apoptosis following hypoxia. Since HIF1α has oncogenic properties, and Cezanne 1 has a pro-survival role in hypoxia, Cezanne 1 has been suggested to be a good target for pharmacological intervention.
  • Cezanne 1 has been shown to have a role in cell proliferation, migration and invasion by antagonizing EGFR (epidermal growth factor receptor) internalisation and degradation. Cezanne 1 and Cezanne 2 were identified in a genetic screen to find a DUB enzyme for EGFR. Cezanne 1 overexpression led to higher levels of phosphorylated EGFR, lower levels of ubiquitylated EGFR and EGFR stabilization. In MDA-MB-231 breast cancer cells, knockdown of Cezanne 1 led to decreased invasion and migration. Analysis of The Cancer Genome Atlas by Pareja et al., showed that Cezanne 1 was overexpressed in breast cancer and amplification of the gene was seen in a third of breast tumours. The level of Cezanne 1 expression correlated with poor prognosis.
  • Although there has been a handful of DUB inhibitors published in the literature, there is a continuing need for compounds and pharmaceutical compositions which inhibit DUBs such as Cezanne 1 and USP30 for the treatment of cancer and other indications where DUB activity is observed.
    • SUMMARY OF THE INVENTION
  • In accordance with a first aspect of the invention there is provided a compound of formula (I)
  • Figure US20180362460A1-20181220-C00002
  • or a pharmaceutically acceptable salt thereof, wherein:
  • R1a, R1b, R1c and R1d each independently represent hydrogen or an optionally substituted C1-C6 alkyl, or R1a is linked to R1b to form an optionally substituted cycloalkyl ring, or R1d is linked to R1c or R1e to form an optionally substituted cycloalkyl ring;
  • R1e and R1f each independently represent hydrogen, fluorine, cyano, hydroxyl, amino, optionally substituted C1-C6 alkyl, optionally substituted C1-C6 alkoxy or an optionally substituted 5 or 6 membered aryl or heteroaryl ring, or R1e and R1f together form an optionally substituted cycloalkyl ring, or R1e is linked to R1d to form an optionally substituted cycloalkyl ring;
  • A is an optionally substituted 5 to 10 membered heteroaryl or aryl ring.
  • A may represent a 5 to 10 membered heteroaryl or aryl ring substituted with one or more of Q1-(R2)n, wherein:
  • n is 0 or 1;
  • Q1 represents halogen, cyano, oxo, nitro, —OR3, —SR3, —NR3R4, —CONR3R4, —NR3COR4, —NR3CONR4R5, —COR3, —C(O)OR3, —SO2R3, —SO2NR3R4, —NR3SO2R4, —NR3SO2NR4R5, —NR3C(O)OR4, optionally substituted —C1-C6 alkyl, optionally substituted —C1-C6 alkoxy, optionally substituted —C2-C6 alkenyl, optionally substituted —C2-C6 alkynyl, a covalent bond, an oxygen atom, a sulphur atom, —SO—, —SO2—, —CO—, —C(O)O—, —CONR3—, —NR3—, —NR3CO—, —NR3CONR4—, —SO2NR3—, —NR3SO2—, —NR3SO2NR4—, —NR3C(O)O—, —NR3C(O)OR4—, optionally substituted C1-C6 alkylene or optionally substituted —C2-C6 alkenylene;
  • R3, R4 and R5 each independently represent hydrogen, optionally substituted C1-C6 alkyl or optionally substituted C1-C6 alkylene.
  • When n is 1, R2 represents an optionally substituted 3 to 10 membered heterocyclyl, heteroaryl, aryl or cycloalkyl ring. (When n is 0, Q1 is present and R2 is absent).
  • R2 may be optionally substituted with one or more substituents selected from halogen, cyano, oxo, nitro, —OR6, —SR6, —NR6R7, —CONR6R7, —NR6COR7, —NR6CONR7R8, —COR6, —C(O)OR6, —SO2R6, —SO2NR6R7, —NR6SO2R7, —NR6SO2NR7R8, —NR6C(O)OR7, optionally substituted —C1-C6 alkyl, optionally substituted —C1-C6 alkoxy, optionally substituted —C2-C6 alkenyl, optionally substituted —C2-C6 alkynyl, -Q2-R6, -Q2-NR6CONR7R8, -Q2-NR6R7, -Q2-COR6, -Q2-NR6COR7, -Q2-NR6C(O)OR7, -Q2-SO2R6, Q2-CONR6R7, -Q2-CO2R6, -Q2-SO2NR6R7, -Q2-NR6SO2R7 and -Q2-NR6SO2NR7R8; wherein
  • Q2 represents a covalent bond, an oxygen atom, a sulphur atom, —SO—, —SO2—, —CO—, optionally substituted C1-C6 alkylene or optionally substituted C2-C6 alkenylene; and
  • R6, R7, R8 each independently represent hydrogen, optionally substituted C1-C6 alkyl, optionally substituted heterocyclyl, optionally substituted heteroaryl, optionally substituted aryl, or an optionally substituted cycloalkyl.
  • In one aspect, the invention also relates to pharmaceutical compositions comprising the compounds of the present invention and one or more pharmaceutically acceptable excipients.
  • In another aspect, the compounds of the invention are useful for the treatment of cancer.
    • BRIEF DESCRIPTION OF THE FIGURES
  • FIG. 1 provides an image of Cezanne 1 purified from mammalian cells. FLAG-purified protein or the indicated concentrations of BSA were separated by SDS-PAGE and stained with Imperial (Pierce Biotechnology).
  • FIG. 2 is a graph showing proteolytic activity of Cezanne 1 measured using a fluorescence polarisation assay. Various volumes of purified Cezanne 1 as indicated were incubated with a TAMRA labelled peptide linked to ubiquitin via an isopeptide bond.
    •  DETAILED DESCRIPTION OF THE INVENTION
  • The definitions and explanations below are for the terms as used throughout this entire document including both the specification and the claims. Reference to compounds as described herein (e.g. a compound of formula (I)), includes reference to formula (I) and (II) including any sub-generic embodiments thereof, e.g. formula (IA).
  • Where any group of the compounds of formula (I) have been referred to as optionally substituted, this group may be substituted or unsubstituted. Substitution may be by one or more of the specified substituents which may be the same or different. It will be appreciated that the number and nature of substituents will be selected to avoid any sterically undesirable combinations.
  • In the context of the present specification, unless otherwise stated an alkyl, alkylene, alkoxy, alkenyl, or alkynyl substituent (or linker) group or an alkyl, alkenyl moiety in a substituent group may be linear or branched. Alkyl, alkylene, alkenyl and alkenylene chains may also include intervening heteroatoms such as oxygen.
  • Cx-Cy alkyl refers to a saturated aliphatic hydrocarbon group having x-y carbon atoms which may be linear or branched. For example C1-C6 alkyl contains from 1 to 6 carbon atoms and includes C1, C2, C3, C4, C5 and C6. “Branched” means that at least one carbon branch point is present in the group. For example, tert-butyl and isopropyl are both branched groups. Examples of C1-C6 alkyl groups include methyl, ethyl, propyl, 2-methyl-1-propyl, 2-methyl-2-propyl, 2-methyl-1-butyl, 3-methyl-1-butyl, 2-methyl-3-butyl, 2,2-dimethyl-1-propyl, 2-methyl-pentyl, 3-methyl-1-pentyl, 4-methyl-1-pentyl, 2-methyl-2-pentyl, 3-methyl-2-pentyl, 4-methyl-2-pentyl, 2,2-dimethyl-1-butyl, 3,3-dimethyl-1-butyl, 2-ethyl-1-butyl, n-butyl, isobutyl, tert-butyl, n-pentyl, isopentyl, neopentyl and n-hexyl. C1-C6 alkyl, C1-C4 alkyl and C1-C3 alkyl within the definitions of R1a, R1b, R1c, R1d, R1e, R1f, R3, R4, R5, R6, R7, R8, Q1, and within the definition of substituents for R2, may be unsubstituted or substituted with one or more of the substituents defined herein. Examples of substituted C1-C6 alkyl therefore include CF3, CH2CF3, CH2CN, CH2OH and CH2CH2OH.
  • A Cx-Cy alkylene group or moiety may be linear or branched and refers to a divalent hydrocarbon group having one less hydrogen atom from Cx-Cy alkyl as defined above. C1-C6 alkylene may include intervening heteroatoms such as oxygen, and therefore includes alkyleneoxy groups. Alkyleneoxy as employed herein also extends to embodiments in which the or an oxygen atom (e.g. a single oxygen atom) is located within the alkylene chain, for example CH2CH2OCH2 or CH2OCH2. Examples of C1-C6 alkylene groups include methylene, methyleneoxy, ethylene, ethyleneoxy, n-propylene, n-propyleneoxy, n-butylene, n-butyleneoxy, methylmethylene and dimethylmethylene. Unless stated otherwise, C1-C6 alkylene, C1-C4 alkylene and C1-C3 alkylene within the definitions of R3, R4, R5, Q1 and Q2 may be unsubstituted or substituted with one or more of the substituents defined herein.
  • C2-C6 alkenyl refers to a linear or branched hydrocarbon chain radical containing at least two carbon atoms and at least one double bond and includes C2-C4 alkenyl. Examples of alkenyl groups include ethenyl, propenyl, 2-propenyl, 1-butenyl, 2-butenyl, 1-hexenyl, 2-methyl-1-propenyl, 1,2-butadienyl, 1,3-pentadienyl, 1,4-pentadienyl and 1-hexadienyl. Unless stated otherwise, C2-C6 alkenyl and C2-C4 alkenyl within the definitions of Q1 and within the definition of substituents for R2, may be unsubstituted or substituted with one or more of the substituents defined herein.
  • C2-C6 alkenylene refers to linear or branched hydrocarbon group having one less hydrogen atom from C2-C6 alkenyl as defined above. Examples of C2-C6 alkenylene include ethenylene, propenylene and butenylene. Unless stated otherwise, C2-C6 alkenylene and C2-C4 alkenylene within the definition of substituents for Q1 and Q2, may be unsubstituted or substituted with one or more of the substituents defined herein.
  • C2-C6 alkynyl refers to a linear or branched hydrocarbon chain radical containing at least two carbon atoms and at least one triple bond. Examples of alkenyl groups include ethynyl, propynyl, 2-propynyl, 1-butynyl, 2-butynyl and 1-hexynyl. Unless specified otherwise, C2-C6 alkynyl, within the definitions of Q1 and within the definition of substituents for R2, may be unsubstituted or substituted with one or more of the substituents defined herein.
  • C1-C6 alkoxy refers to a group or part of a group having an —O—Cx-Cy alkyl group according to the definition of Cx-Cy alkyl above. C1-C6 alkoxy contains from 1 to 6 carbon atoms and includes C1, C2, C3, C4, C5 and C6. Examples of C1-C6 alkoxy include methoxy, ethoxy, propoxy, isopropoxy, butoxy, pentoxy and hexoxy. Alkoxy as employed herein also extends to embodiments in which the or an oxygen atom (e.g. a single oxygen atom) is located within the alkyl chain, for example CH2CH2OCH3 or CH2OCH3. Thus the alkoxy may be linked through carbon to the remainder of the molecule, for example, —CH2CH2OCH3, or alternatively, the alkoxy is linked through oxygen to the remainder of the molecule, for example —OC1-6 alkyl. In certain instances, the alkoxy may be linked through oxygen to the remainder of the molecule but the alkoxy group contains a further oxygen atom, for example —OCH2CH2OCH3. Unless specified otherwise, C1-C6 alkoxy and C1-C3 alkoxy within the definitions R1e, R1f, Q1, and within the definition of substituents for R2, may be unsubstituted or substituted with one or more of the substituents defined herein. Examples of substituted C1-C6 alkoxy therefore include OCF3, OCHF2, OCH2CF3, CH2CH2OCH3 and CH2CH2OCH2CH3.
  • The term “halogen” or “halo” refers to chlorine, bromine, fluorine or iodine atoms, in particular chlorine or fluorine atoms.
  • The term “oxo” means ═O.
  • For the avoidance of doubt it will be understood that the cycloalkyl, heterocyclyl, aryl and heteroaryl rings disclosed herein and within the definitions of R1a, R1b, R1c, R1d, R1e, R1f, R2, R6, R7, R8, ring A, and within the definition of substituents for R2, do not include any unstable ring structures or, in the case of heteroaryl and heterocyclic rings systems, any O—O, O—S or S—S bonds. The ring systems may be monocyclic or bicyclic. Bicyclic ring systems include bridged, fused and spiro ring systems. A substituent if present may be attached to any suitable ring atom which may be a carbon atom or, in the case of heteroaryl and heterocyclic ring systems, a heteroatom. Substitution on a ring may also include a change in the ring atom at the position of the substitution. For example, substitution on a phenyl ring may include a change in the ring atom at the position of substitution from carbon to nitrogen, resulting in a pyridine ring.
  • “cycloalkyl” refers to a monocyclic saturated or partially unsaturated, non-aromatic ring, wherein all of the ring atoms are carbon, and having the number of ring atoms as indicated. For example C3-C10 cycloalkyl refers to a monocyclic or bicyclic hydrocarbon ring containing 3 to 10 carbon atoms. Examples of C3-C10 cycloalkyl are cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl and decahydronaphthalenyl. Bicyclic cycloalkyl groups include bridged ring systems such as bicycloheptane and bicyclooctane. Unless specified otherwise, cycloalkyl within the definitions of R1a, R1b, R1c, R1d, R1e, R1f, R2, R6, R7, R8, and within the definition of substituents for R2, may be unsubstituted or substituted with one or more of the substituents defined herein.
  • An “aryl” group/moiety refers to any monocyclic or bicyclic hydrocarbon group comprising at least one aromatic group and having from 5 to 10 carbon atom ring members. Examples of aryl groups include phenyl and naphthyl. Bicyclic rings may be fused aromatic rings where both rings are aromatic, for example, naphthalenyl. Preferred aryl groups are phenyl and naphthyl, more preferably 5 phenyl. Unless specified otherwise, aryl within the definitions of R1e, R1f, R2, R6, R7, R8, ring A, and within the definition of substituents for R2, may be unsubstituted or substituted with one or more of the substituents defined herein.
  • “Heteroaryl” as used herein means a polyunsaturated, monocyclic or bicyclic 5 to 10 membered aromatic moiety containing at least one and up to 5 heteroatoms, particularly 1, 2 or 3 heteroatoms selected from N, O and S, and the remaining ring atoms are carbon atoms, in stable combinations known to the skilled person. Heteroaryl ring nitrogen and sulphur atoms are optionally oxidised, and the nitrogen atom(s) are optionally quaternized. A heteroaryl ring can be a single aromatic ring or a fused bicyclic ring where the bicyclic ring system can be aromatic, or one of the fused rings is aromatic and the other is at least partially saturated. In one example, a bicyclic heteroaryl is one in which the entire fused ring system is aromatic. Examples of fused rings where one of the rings is aromatic and the other is at least partially saturated include tetrahydropyridopyrazinyl, tetrahydroquinolinyl and tetrahydroisoquinolinyl. In such instances, attachment of the bicyclic ring to the group it is a substituent of relative to the cyanopyrrolidine core, e.g. attachment of ring A via the amide group, is from the aromatic ring of the bicycle. A bicyclic heteroaryl can have the at least one heteroatom in either of the fused rings. For example, a bicyclic ring with an aromatic ring fused to a partially saturated ring may contain the at least one heteroatom in the aromatic ring or the partially saturated ring. Attachment of the bicyclic ring to the group it is a substituent of may be via either a heteroatom containing ring or a carbon only containing ring. The point of attachment of heteroaryl to the group it is a substituent of can be via a carbon atom or a heteroatom (e.g. nitrogen). Examples of heteroaryl rings include pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, furyl, pyrrolyl, oxazolyl, thiazolyl, pyrazolyl, triazolyl, tetrazolyl, indolyl, indolizinyl, isoindolyl, purinyl, furazanyl, imidazolyl, indazolyl, isothiazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, thiadiazolyl, benzofuranyl, isobenzofuranyl, benzothiophenyl, isobenzothiophenyl, benzimidazolyl, benzothiazolyl, napthyridinyl, pteridinyl, pyrazinyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl, imidazopyridinyl, pyrazolopyridinyl, thiazolopyridinyl, triazinyl, dihydrophyridinyl, dihydropyrrolopyridinyl, indolinyl, isoindolinyl, quinoxalinyl, benzomorpholinyl, tetrahydropyridopyrazinyl, tetrahydroquinolinyl and tetrahydroisoquinolinyl. Unless specified otherwise, heteroaryl within the definitions of R1e, R1f, R2, R6, R7, R8, ring A, and within the definition of substituents for R2, may be unsubstituted or substituted with one or more of the substituents defined herein.
  • “Heterocyclyl” or “heterocyclic” as used herein in describing a ring means, unless otherwise stated, a monocyclic saturated or partially unsaturated, non-aromatic ring or a bicyclic saturated or partially unsaturated ring, wherein the bicyclic ring system is non-aromatic, the mono- or bicyclic ring having, for example, 3 to 10 members, where at least one member and up to 5 members, particularly 1, 2 or 3 members of the ring are heteroatoms selected from N, O and S, and the remaining ring atoms are carbon atoms, in stable combinations known to those of skill in the art. For example, R2 and R3 may together form a heterocyclic ring which incorporates the amine nitrogen. Heterocyclic ring nitrogen and sulphur atoms are optionally oxidised, and the nitrogen atoms(s) are optionally quaternized. As used herein, the heterocyclic ring may be a fused ring to another ring system to form a bicycle, i.e. one or two of the heterocyclic ring carbons is common to an additional ring system. In instances where the heterocylcyl is a bicyclic ring, the second ring can be aromatic, e.g. a fused phenyl, pyridyl, pyrazolyl, or the like. The bicyclic heterocyclyl can have at least one heteroatom in either of the fused rings. The heterocyclyl may be linked through carbon or a heteroatom to the remainder of the molecule and in instances where the heterocylyl is a bicyclic ring, the link may be via the heteroatom containing ring or the fused ring. In instances where the heterocyclyl is a bicyclic ring where the second ring is aromatic, attachment of the bicyclic group to the group it is a substituent of relative to the cyanopyrrolidine core is from the non-aromatic ring. Examples of heterocyclyl groups include azetidinyl, pyrrolidinyl, piperidinyl, azepanyl, diazepanyl, dihydrofuranyl (e.g. 2,3-dihydrofuranyl, 2,5-dihydrofuranyl), dioxolanyl, morpholinyl, oxazolidinyl, oxazinanyl, indolinyl, isoindolinyl, piperazinyl, tetrahydrofuranyl, thiomorpholinyl, dihydropyranyl (e.g. 3,4-dihydropyranyl, 3,6-dihydropyranyl), homopiperazinyl, dioxanyl, hexahydropyrimidinyl, pyrazolinyl, pyrazolidinyl, 4H-quinolizinyl, quinuclidinyl, tetrahydropyranyl, tetrahydropyridinyl, tetrahydropyrimidinyl, tetrahydrothiophenyl, thiazolidinyl, benzopyranyl, tetrahydroquinolinyl, benzomorpholinyl and tetrahydroisoquinolinyl. Unless specified otherwise, heterocyclyl within the definitions of R2, R6, R7, R8 and within the definition of substituents for R2, may be unsubstituted or substituted with one or more of the substituents defined herein. Examples of substituted heterocyclyl rings include for example 4,5-dihydro-1H-maleimido,tetramethylenesulfoxide and hydantoinyl.
  • “Optionally substituted” as applied to any group means that the said group may if desired be substituted with one or more substituents (e.g., 1, 2, 3 or 4 substituents) which may be the same or different.
  • Examples of suitable substituents for “substituted” and “optionally substituted” C1-C6 alkyl (including C1-C4 alkyl, C1-C3 alkyl and C1-C2 alkyl) and C1-C6 alkoxy (including C1-C4 alkoxy, C1-C3 alkoxy and C1-C2 alkoxy) and C2-C6 alkenyl (including C2-C4 alkenyl) and C2-C6 alkynyl (including C2-C4 alkynyl), for example within the definitions of R1a, R1b, R1c, R1d, R1e, R1f, R3, R4, R5, R6, R7, R8, Q1, and within the definition of substituents for R2, and C1-C6 alkylene (including C1-C3 alkylene) and C2-C6 alkenylene, for example within the definitions of R3, R4, R5, Q1 and Q2, include halogen, hydroxyl, thiol, cyano, amino, nitro and SF5 (a known mimetic of nitro), in particular, halogen (preferably fluorine or chlorine), hydroxyl and cyano.
  • Examples of suitable substituents for “substituted” and “optionally substituted” rings, i.e. cycloalkyl, heterocyclyl, aryl and heteroaryl rings, for example within the definitions of R1a, R1b, R1c, R1d, R1e, R1f, R2, R6, R7, R8, ring A, and within the definition of substituents for R2, include halogen, cyano, oxo, nitro, amino, hydroxy, C1-C6 alkyl or C1-C3 alkyl, C1-C6 alkoxy or C1-C3 alkoxy, aryl, heteroaryl, heterocyclyl, C3-C6 cycloalkyl, C1-3 alkylamino, C2-6 alkenylamino, di-C1-C3 alkylamino, C1-C3 acylamino, di-C1-C3 acylamino, carboxy, C1-C3 alkoxycarbonyl, carboxamidyl, carbamoyl, mono-C1-3 carbamoyl, di-C1-3 carbamoyl or any of the above in which a hydrocarbyl moiety is itself substituted by halogen, e.g. fluorine, hydroxyl, cyano, amino, nitro or SF5 (a known mimetic of nitro). In groups containing an oxygen atom such as hydroxy and alkoxy, the oxygen atom can be replaced with sulphur to make groups such as thio (SH) and thio-alkyl (S-alkyl). Optional substituents therefore include groups such as S-methyl. In thio-alkyl groups, the sulphur atom may be further oxidised to make a sulfoxide or sulfone, and thus optional substituents therefore includes groups such as S(O)-alkyl and S(O)2-alkyl.
  • Examples of suitable substituents for “substituted” and “optionally substituted” rings include in particular, fluorine, chlorine, oxo, cyano, C1-C3 alkyl, C1-C3 alkoxy, heterocyclyl, cycloalkyl, heteroary or aryl, wherein the alkyl or alkoxy is optionally substituted with one or more (e.g. one, two or three) substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF5.
  • Substituted groups thus include for example Br, Cl, F, CN, Me, Et, Pr, Bu, i-Bu, OMe, OEt, OPr, C(CH3)3, CH(CH3)2, CF3, OCF3, C(O)NHCH3, cyclopropyl, phenyl, etc. In the case of aryl groups, the substitutions may be in the form of rings from adjacent carbon atoms in the aryl ring, for example cyclic acetals such as O—CH2—O.
  • The term “treat” or “treating” or “treatment” includes prophylaxis and means to ameliorate, alleviate symptoms, eliminate the causation of the symptoms either on a temporary or permanent basis, or to prevent or slow the appearance of symptoms of the named disorder or condition. The compounds of the invention are useful in the treatment of humans and non-human animals.
  • The dose of the compound is that amount effective to prevent occurrence of the symptoms of the disorder or to treat some symptoms of the disorder from which the patient suffers. By “effective amount” or “therapeutically effective amount” or “effective dose” is meant that amount sufficient to elicit the desired pharmacological or therapeutic effects, thus resulting in effective prevention or treatment of the disorder. Prevention of the disorder is manifested by delaying the onset of the symptoms of the disorder to a medically significant extent. Treatment of the disorder is manifested by a decrease in the symptoms associated with the disorder or an amelioration of the reoccurrence of the symptoms of the disorder.
  • Pharmaceutically acceptable salts of the compounds of the invention include but are not limited to addition salts (for example phosphates, nitrates, sulphates, borates, acetates, maleates, citrates, fumarates, succinates, methanesulphonates, benzoates, salicylates and hydrohalides), salts derived from organic bases (such as lithium, potassium and sodium), salts of amino acids (such as glycine, alanine, valine, leucine, isoleucine, cysteine, methionine and proline), inorganic bases (such as triethylamine, hydroxide, choline, thiamine and N—N′-diacetylethylenediamine). Other pharmaceutically acceptable salts include ammonium salts, substituted ammonium salts and aluminium salts. Further pharmaceutically acceptable salts include quaternary ammonium salts of the compounds of the invention.
  • General methods for the production of salts are well known to the person skilled in the art. Such salts may be formed by conventional means, for example by reaction of a free acid or a free base form of a compound with one or more equivalents of an appropriate acid or base, optionally in a solvent, or in a medium in which the salt is insoluble, followed by removal of said solvent, or said medium, using standard techniques (e.g. in vacuo, by freeze-drying or by filtration). Salts may also be prepared by exchanging a counter-ion of a compound in the form of a salt with another counter-ion, for example using a suitable ion exchange resin.
  • Where compounds of the invention exist in different enantiomeric and/or diastereoisomeric forms, the invention relates to these compounds prepared as isomeric mixtures or racemates whether present in an optically pure form or as mixtures with other isomers. Enantiomers differ only in their ability to rotate plane-polarized light by equal amounts in opposite directions and are denoted as the (+)/(S) or (−)/(R) forms respectively. Individual enantiomers or isomers may be prepared by methods known in the art, such as optical resolution of products or intermediates (for example chiral chromatographic separation e.g. chiral HPLC, or an asymmetric synthesis approach). Similarly where compounds of the invention exist as alternative tautomeric forms e.g. keto/enol, amide/imidic acid, the invention relates to the individual tautomers in isolation, and to mixtures of the tautomers in all proportions.
  • Included herein is the compound according to formula (II)
  • Figure US20180362460A1-20181220-C00003
  • or a pharmaceutically acceptable salt thereof, wherein:
  • R1a, R1b, R1c and R1d each independently represent hydrogen or an optionally substituted C1-C6 alkyl, or R1a is linked to R1b to form an optionally substituted cycloalkyl ring, or R1d is linked to R1c or R1e to form an optionally substituted cycloalkyl ring;
  • R1e and R1f each independently represent hydrogen, fluorine, cyano, hydroxyl, amino, optionally substituted C1-C6 alkyl, optionally substituted C1-C6 alkoxy or an optionally substituted 5 or 6 membered ring, or R1e and R1f together form an optionally substituted cycloalkyl ring, or R1e is linked to R1d to form an optionally substituted cycloalkyl ring;
  • A is an optionally substituted 5 to 10 membered heteroaryl or aryl ring.
  • Isotopes
  • The compounds described herein may contain one or more isotopic substitutions, and a reference to a particular element includes within its scope all isotopes of the element. For example, a reference to hydrogen includes within its scope 1H, 2H (D), and 3H (T). Similarly, references to carbon and oxygen include within their scope respectively 12C, 13C and 14C and 16O and 18O. Examples of isotopes include 2H, 3H, 11C, 13C, 14C, 36C, 18F, 123I, 125I, 13N, 15N, 15O, 17O, 18O, 32P and 35S.
  • In an analogous manner, a reference to a particular functional group also includes within its scope isotopic variations, unless the context indicates otherwise. For example, a reference to an alkyl group such as an ethyl group also covers variations in which one or more of the hydrogen atoms in the group is in the form of a deuterium or tritium isotope, e.g. as in an ethyl group in which all five hydrogen atoms are in the deuterium isotopic form (a perdeuteroethyl group).
  • The isotopes may be radioactive or non-radioactive. In one embodiment, the compounds contain no radioactive isotopes. Such compounds are preferred for therapeutic use. In another embodiment, however, the compounds may contain one or more radioisotopes. Compounds containing such radioisotopes may be useful in a diagnostic context.
  • Certain isotopically labelled compounds of formula (I), for example, those incorporating a radioactive isotope, are useful in drug and/or substrate tissue distribution studies. The radioactive isotopes i.e. 3H and 14C are particularly useful for this purpose in view of their ease of incorporation and ready means of detection. Substitution with heavier isotopes i.e. 2H, may afford certain therapeutic advantages resulting from greater metabolic stability, for example, increased in vivo half-life or reduced dosage requirements, and hence may be preferred in some circumstances. Substitution with positron emitting isotopes, such as 11C, 18F, 15O and 13N, can be useful in Positron Emission Topography (PET) studies for examining receptor occupancy. Isotopically labelled compounds of formula (I) can generally be prepared by conventional techniques known to those skilled in the art or by processes analogous to those described in the accompanying examples and preparations using an appropriate isotopically labelled reagent in place of the non-labelled reagent previously employed.
  • Crystalline and Amorphous Forms
  • The compounds of formula (I) may exist in crystalline or amorphous form and some of the crystalline forms may exist as polymorphs, which are included within the scope of the present invention. Polymorphic forms of compounds of formula (I) may be characterised and differentiated using a number of conventional analytical techniques, including, but not limited to, infra-red spectra, Raman spectra, X-ray powder diffraction, differential scanning calorimetry, thermogravimetric analysis and solid state nuclear magnetic resonance.
  • Accordingly, in further embodiments, the invention provides a compound according to any described embodiments in a crystalline form. The compound may be from 50% to 100% crystalline, and more particularly is at least 50% crystalline, or at least 60% crystalline, or at least 70% crystalline, or at least 80% crystalline, or at least 90% crystalline, or at least 95% crystalline, or at least 98% crystalline, or at least 99% crystalline, or at least 99.5% crystalline, or at least 99.9% crystalline, for example 100% crystalline. The compound may alternatively be in an amorphous form.
  • The invention described herein relates to all crystal forms, solvates and hydrates of any of the disclosed compounds however so prepared. To the extent that any of the compounds disclosed herein have acid or basic centres such as carboxylates or amino groups, then all salt forms of said compounds are included herein. In the case of pharmaceutical uses, the salt should be seen as being a pharmaceutically acceptable salt.
  • The invention relates to any solvates of the compounds and their salts. Preferred solvates are solvates formed by the incorporation into the solid state structure (e.g. crystal structure) of the compounds of the invention of molecules of a non-toxic pharmaceutically acceptable solvent (referred to below as the solvating solvent). Examples of such solvents include water, alcohols (such as ethanol, isopropanol and butanol) and dimethylsulfoxide. Solvates can be prepared by recrystallising the compounds of the invention with a solvent or mixture of solvents containing the solvating solvent. Whether or not a solvate has been formed in any given instance can be determined by subjecting crystals of the compound to analysis using well known and standard techniques such as thermogravimetric analysis (TGE), differential scanning calorimetry (DSC) and X-ray crystallography.
  • The solvates can be stoichiometric or non-stoichiometric solvates. Particular solvates may be hydrates, and examples of hydrates include hemihydrates, monohydrates and dihydrates. For a more detailed discussion of solvates and the methods used to make and characterise them, see Bryn et al., Solid-State Chemistry of Drugs, Second Edition, published by SSCI, Inc of West Lafayette, Ind., USA, 1999, ISBN 0-967-06710-3.
  • The invention relates to pharmaceutically functional derivatives of compounds as defined herein including ester derivatives and/or derivatives that have, or provide for, the same biological function and/or activity as any relevant compound of the invention. Thus, for the purposes of this invention, the term also includes prodrugs of compounds as defined herein.
  • The term “prodrug” of a relevant compound includes any compound that, following oral or parenteral administration, is metabolised in vivo to form that compound in an experimentally-detectable amount, and within a predetermined time (e.g. within a dosing interval of between 6 and 24 hours (i.e. once to four times daily).
  • Prodrugs of compounds may be prepared by modifying functional groups present on the compound in such a way that the modifications are cleaved, in vivo when such prodrug is administered to a mammalian subject. The modifications typically are achieved by synthesizing the parent compound with a prodrug substituent. Prodrugs include compounds wherein a hydroxyl, amino, sulfhydryl, carboxyl or carbonyl group in a compound is bonded to any group that may be cleaved in vivo to regenerate the free hydroxyl, amino, sulfhydryl, carboxyl or carbonyl group, respectively.
  • Examples of prodrugs include, but are not limited to, esters and carbamates of hydroxyl functional groups, ester groups of carboxyl functional groups, N-acyl derivatives and N-Mannich bases. General information on prodrugs may be found e.g. in Bundegaard, H. “Design of Prodrugs” p. 1-92, Elsevier, New York-Oxford (1985).
  • Compounds of the invention may be metabolised in vivo. Metabolites of compounds of formula (I) are also within the scope of the present invention. The term ‘metabolites’ refers to all molecules derived from any of the compounds according to the present invention in a cell or organism, preferably mammal. Preferably the term relates to molecules which differ from any molecule which is present in any such cell or organism under physiological conditions.
  • A treatment defined herein may be applied as a sole therapy of may involve, in addition to the compounds of the invention, conventional surgery or radiotherapy or chemotherapy. Furthermore, compounds of formula (I) can also be used in combination with existing therapeutic agents for the treatment of conditions associated with cancer, including small molecule therapeutics or antibody based therapeutics.
  • The compounds described herein are characterised by a cyanopyrrolidine core with an amide group and fluorine attached to the same position on the cyannopyrrolidine ring, wherein the amide group is substituted with an optionally substituted aryl or heteroaryl ring.
  • In accordance with a first aspect of the invention there is provided a compound of formula (I)
  • Figure US20180362460A1-20181220-C00004
  • or a pharmaceutically acceptable salt thereof, wherein:
  • R1a, R1b, R1c and R1d each independently represent hydrogen or an optionally substituted C1-C6 alkyl, or R1a is linked to R1b to form an optionally substituted C3-C6 cycloalkyl ring, or R1d is linked to R1c or R1e to form an optionally substituted C3-C6 cycloalkyl ring;
  • R1e and R1f each independently represent hydrogen, fluorine, cyano, hydroxyl, amino, optionally substituted C1-C6 alkyl, optionally substituted C1-C6 alkoxy or an optionally substituted 5 or 6 membered heteroaryl or aryl ring, or R1e and R1f together form an optionally substituted C3-C6 cycloalkyl ring, or R1e is linked to R1d to form an optionally substituted C3-C6 cycloalkyl ring;
  • A is an optionally substituted monocyclic or bicyclic 5 to 10 membered heteroaryl or aryl ring.
  • R1a, R1b, R1c, Rid may each independently represent hydrogen or optionally substituted C1-C6 alkyl. In particular, R1a, R1b, R1c, R1d may each independently represent hydrogen or C1-C3 alkyl (e.g. methyl or ethyl). R1a may be hydrogen or C1-C3 alkyl and R1b may be hydrogen. R1c may be hydrogen or C1-C3 alkyl and R1d may be hydrogen. The alkyl may be unsubstituted or substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF5. In particular R1aR1b, R1c, Rid each represent hydrogen.
  • R1a may represent hydrogen. R1a may represent C1-C6 alkyl. R1a may represent C1-C3 alkyl, for example, methyl or ethyl. When R1a represents C1-C6 alkyl, R1b, R1c, R1d, R1e and R1f may each represent hydrogen. The alkyl may be unsubstituted or substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF5, in particular fluorine.
  • R1b may represent hydrogen. R1b may represent C1-C6 alkyl. R1b may represent C1-C3 alkyl, for example, methyl or ethyl. When R1b represents C1-C6 alkyl, R1a, R1c, R1d, R1e and R1f may each represent hydrogen. The alkyl may be unsubstituted or substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF5, in particular fluorine.
  • R1c may represent hydrogen. R1c may represent C1-C6 alkyl. R1c may represent C1-C3 alkyl, for example, methyl or ethyl. When R1c represents C1-C6 alkyl, R1a, R1b, R1d, R1e and R1f may each represent hydrogen. The alkyl may be unsubstituted or substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF5, in particular fluorine.
  • R1d may represent hydrogen. R1d may represent C1-C6 alkyl. R1d may represent C1-C3 alkyl, for example, methyl or ethyl. When R1d represents C1-C6 alkyl, R1a, R1b, R1c, R1e and R1f may each represent hydrogen. The alkyl may be unsubstituted or substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF5, in particular fluorine.
  • Alternatively, R1a and R1b may together form a cycloalkyl ring. In addition, or alternatively, R1c and R1d may together form a cycloalkyl ring. The cycloalkyl ring can contain 3, 4, 5 or 6 atoms, in particular 3 or 4 atoms. When R1b and R1c together form a C3-C6 cycloalkyl ring, R1a, R1d, R1e and R1f may be hydrogen. When R1d and R1e together form a cycloalkyl ring, R1a, R1b, R1c and R1f may each be hydrogen.
  • R1e may represent hydrogen, fluorine, cyano, hydroxyl, amino, optionally substituted C1-C6 alkyl, optionally substituted C1-C6 alkoxy or an optionally substituted 5 or 6 membered heteroaryl or aryl ring. The alkyl and alkoxy may be substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF5. The heteroaryl or aryl ring may be unsubstituted or substituted with halogen, cyano, oxo, nitro, amino, hydroxy, C1-C6 alkyl or C1-C6 alkoxy. In particular, R1e can represent hydrogen, fluorine, C1-C3 alkyl or substituted C1-C3 alkoxy. R1e can represent fluorine. R1e can represent methyl. R1e can represent methoxy. R1e can represent CF3. R1e can represent OCF3. When R1e represents fluorine, cyano, hydroxyl, amino, optionally substituted C1-C6 alkyl, optionally substituted C1-C6 alkoxy or an optionally substituted 5 or 6 membered heteroaryl or aryl ring, R1a, R1b, R1c, R1d and R1f may each represent hydrogen. Alternatively, R1e represents hydrogen.
  • R1f may represent hydrogen fluorine, cyano, hydroxyl, amino, optionally substituted C1-C6 alkyl, optionally substituted C1-C6 alkoxy, or an optionally substituted 5 or 6 membered heteroaryl or aryl ring. The alkyl and alkoxy may be substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF5. The heteroaryl or aryl ring may be unsubstituted or substituted with halogen, cyano, oxo, nitro, amino, hydroxy, C1-C6 alkyl or C1-C6 alkoxy. In particular, R1f can represent hydrogen fluorine, unsubstituted or substituted C1-C3 alkyl or unsubstituted or substituted C1-C3 alkoxy. R1f can represent fluorine. R1f can represent methyl. R1f can represent methoxy. R1f can represent CF3. R1f can represent OCF3. When R1f represents fluorine, cyano, hydroxyl, amino, optionally substituted C1-C6 alkyl or optionally substituted C1-C6 alkoxy or an optionally substituted 5 or 6 membered heteroaryl or aryl ring, R1a, R1b, R1c, R1d and R1e may each represent hydrogen. Alternatively, R1f represents hydrogen.
  • Alternatively, R1e and R1f may together form a cycloalkyl ring. Alternatively, R1e and R1d may together form a cycloalkyl ring. The cycloalkyl ring can contain 3, 4, 5 or 6 atoms, in particular 3 or 4 atoms. When R1e and R1f together form a C3-C6 cycloalkyl ring, R1a, R1b, R1c and R1d may be hydrogen. When R1e and R1d together form a cycloalkyl ring, R1a, R1b, R1c and R1f may each be hydrogen.
  • The cycloalkyl rings within the definitions of R1a, R1b, R1c, R1d, R1e and R1f may be unsubstituted or substituted with one or more substituents selected from halogen, cyano, oxo, nitro, amino, hydroxy, C1-C3 alkyl, C1-C3 alkoxy, C1-3 alkylamino, C2-6 alkenylamino, C1-C3 acylamino, carboxy, C1-C3 alkoxycarbonyl, carboxamidyl, carbamoyl, wherein any hydrocarbyl moiety may itself be substituted by one or more halogen, in particular fluorine. In particular, the cycloalkyl ring may be unsubstituted or substituted with one or two substituents selected from halogen, cyano, oxo, nitro, amino, hydroxy, C1-C3 alkyl and C1-C3 alkoxy, wherein the alkyl and alkoxy may be substituted with one or more halogen, in particular fluorine.
  • One of R1a, R1b, R1c, R1d, R1e and R1f may be other than hydrogen, and the remaining are each hydrogen.
  • Two of R1a, R1b, R1c, R1d, R1e and R1f may be other than hydrogen, and the remaining are each hydrogen.
  • Three of R1a, R1b, R1c, R1d, R1e and R1f may be other than hydrogen, and the remaining are each hydrogen.
  • Four of R1a, R1b, R1c, R1d, R1e and R1f may be other than hydrogen, and the remaining are each hydrogen.
  • Five of R1a, R1b, R1c, R1d, R1e and R1f may be other than hydrogen, and the remaining are each hydrogen.
  • Six of R1a, R1b, R1c, R1d, R1e and R1f may be other than hydrogen, and the remaining are each hydrogen.
  • When one, two, three, four, five or six of R1a, R1b, R1c, R1d, R1e and R1f are other than hydrogen, the remaining R groups represent a group in accordance with the definitions above. In particular, one, two, three or four of R1a, R1b, R1c, R1d, R1e and R1f may be other than hydrogen and the remaining each represent hydrogen. More particularly, one or two of R1a, R1b, R1c, R1d, R1e and R1f may be other than hydrogen and the remaining each represent hydrogen.
  • The compounds may be in the form where R1a, R1b, R1c, R1d, R1e and R1f are each hydrogen. In such cases the compounds may be of formula (IA):
  • Figure US20180362460A1-20181220-C00005
  • or a pharmaceutically acceptable salt thereof, wherein A is an optionally substituted 5 to 10 membered heteroaryl or aryl ring.
  • The heteroaryl or aryl ring of ring A may be defined according to the definition of heteroaryl and aryl ring found herein and may be monocyclic or bicyclic. Where the ring is bicyclic, the second ring may be aromatic, or may be partly saturated, and thus not every atom in the 5 to 10 membered ring need be in an aryl system, there must be at least one aryl or heteroaryl ring within the 5 to 10 atoms, and it is this ring that is attached to the amide nitrogen.
  • A represents a 5 to 10 membered (e.g. 5, 6, 7, 8, 9 or 10 membered) monocyclic or fused bicyclic heteroaryl or aryl ring which may be optionally substituted with one or more (e.g. one, two, three or four) of -Q1-(R2)n, in particular one or two of -Q1-(R2)n.
  • In particular, A may represent a 5 or 6 membered heteroaryl or aryl ring which may be optionally substituted with one or more (e.g. one, two, three or four) of -Q1(R2)n.
  • Alternatively, A may represent a 9 or 10 membered bicyclic heteroaryl or aryl ring which may be optionally substituted with one or more (e.g. one, two, three or four) of -Q1(R2)n.
  • When A is a heteroaryl ring, the ring may be monocyclic or bicyclic and comprise one or more (e.g. 1, 2 or 3) heteroatoms independently selected from nitrogen, oxygen and sulphur. In particular, the heteroaryl ring may contain at least one nitrogen atom, for example, 1, 2 or 3 nitrogen atoms, preferably 1 or 2 nitrogen heteroatoms. Examples of nitrogen containing heteroaryl rings include pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, pyrrolyl, oxazolyl, thiazolyl, pyrazolyl, triazolyl, tetrazolyl, indolyl, indolizinyl, isoindolyl, indolinyl, purinyl, furazanyl, imidazolyl, indazolyl, isothiazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, thiadiazolyl, benzimidazolyl, benzothiazolyl, napthyridinyl, pteridinyl, pyrazinyl, 4H-quinolizinyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl, imidazopyridinyl, pyrazolopyridinyl, thiazolopyridinyl, isoindolinyl, triazinyl, dihydrophyridinyl, quinoxalinyl, benzomorpholinyl, dihydropyrrolopyridinyl, tetrahydropyridopyrazinyl, tetrahydroquinolinyl and tetrahydroisoquinolinyl.
  • For example, nitrogen containing heteroaryl rings include pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, pyrrolyl, oxazolyl, thiazolyl, pyrazolyl, triazolyl, tetrazolyl, indolyl, indolizinyl, isoindolyl, indolinyl, purinyl, furazanyl, imidazolyl, indazolyl, isothiazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, thiadiazolyl, benzimidazolyl, benzothiazolyl, napthyridinyl, pteridinyl, pyrazinyl, 4H-quinolizinyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl, imidazopyridinyl, pyrazolopyridinyl, thiazolopyridinyl, isoindolinyl, triazinyl, dihydrophyridinyl, quinoxalinyl and benzomorpholinyl.
  • The optionally substituted 5 to 10 membered heteroaryl or aryl ring may be selected from pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, furyl, pyrrolyl, oxazolyl, thiazolyl, pyrazolyl, triazolyl, tetrazolyl, indolyl, indolizinyl, isoindolyl, purinyl, furazanyl, imidazolyl, indazolyl, isothiazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, thiadiazolyl, benzofuranyl, isobenzofuranyl, benzothiophenyl, isobenzothiophenyl, benzimidazolyl, benzothiazolyl, napthyridinyl, pteridinyl, pyrazinyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl, imidazopyridinyl, pyrazolopyridinyl, thiazolopyridinyl, triazinyl, dihydrophyridinyl, dihydropyrrolopyridinyl, indolinyl, isoindolinyl, quinoxalinyl, benzomorpholinyl, tetrahydropyridopyrazinyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, phenyl, naphthyl and naphthalenyl.
  • For example, the optionally substituted 5 to 10 membered heteroaryl or aryl ring may be selected from pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, furyl, pyrrolyl, oxazolyl, thiazolyl, pyrazolyl, triazolyl, tetrazolyl, indolyl, indolizinyl, isoindolyl, purinyl, furazanyl, imidazolyl, indazolyl, isothiazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, thiadiazolyl, benzofuranyl, isobenzofuranyl, benzothiophenyl, isobenzothiophenyl, benzimidazolyl, benzothiazolyl, napthyridinyl, pteridinyl, pyrazinyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl, imidazopyridinyl, pyrazolopyridinyl, thiazolopyridinyl, triazinyl, dihydrophyridinyl, quinoxalinyl, benzomorpholinyl, phenyl, naphthyl and naphthalenyl.
  • In instances where ring A is a fused bicyclic ring where one of the rings is aromatic and the other is at least partially saturated, attachment to the cyanopyrrolidine ring via the amide is from the aromatic ring of the bicycle.
  • In particular, ring A is selected from thiazolyl, imidazolyl, isoxazolyl, pyrazolyl, phenyl, benzothiazolyl, imidazopyridinyl and quinolinyl.
  • In all cases described herein, ring A may be unsubstituted or substituted with one or more -Q1-(R2) wherein each occurrence of -Q1-(R2)n is the same or different, and wherein:
  • n is 0 or 1;
  • Q1 represents halogen, cyano, oxo, nitro, —OR3, —SR3, —NR3R4, —CONR3R4, —NR3COR4, —NR3CONR4R5, —COR3, —C(O)OR3, —SO2R3, —SO2NR3R4, —NR3SO2R4, —NR3SO2NR4R5, —NR3C(O)OR4, optionally substituted —C1-C6 alkyl, optionally substituted —C1-C6 alkoxy, optionally substituted —C2-C6 alkenyl, optionally substituted —C2-C6 alkynyl, a covalent bond, an oxygen atom, a sulphur atom, —SO—, —SO2—, —CO—, —C(O)O—, —CONR3—, —NR3—, —NR3CO—, —NR3CONR4—, —SO2NR3—, —NR3SO2—, —NR3SO2NR4—, —NR3C(O)O—, —NR3C(O)OR4—, optionally substituted C1-C6 alkylene or optionally substituted —C2-C6 alkenylene;
  • R3, R4 and R5 each independently represent hydrogen, optionally substituted C1-C6 alkyl or optionally substituted C1-C6 alkylene.
  • When n is 1, R2 represents an optionally substituted 3 to 10 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring (when n is 0, Q1 is present and R2 is absent).
  • Ring A may be unsubstituted or substituted with one, two, three or four of -Q1-(R2)n.
  • In particular, ring A is either unsubstituted or substituted with one or two of -Q1-(R2)n. Each occurrence of -Q1-(R2)n may be the same or different. Alternatively, ring A may be either unsubstituted or substituted with one of -Q1-(R2)n. Q1, R2 and n are as defined herein.
  • In all cases described herein, Q1 may be selected from halogen (e.g. fluorine, chlorine or bromine), cyano, oxo, nitro, —OR3 (e.g hydroxyl), —SR3 (e.g. thiol), —NR3R4 (e.g. amino or N,N-dimethylamino), —CONR3R4 (e.g. amido), —NR3COR4 (N-acetyl), —NR3CONR4R5, —COR3 (e.g. acetyl), —C(O)OR3 (e.g. methoxycarbonyl or ethoxycarbonyl), —SO2R3 (e.g. methyl sulphonyl), —SO2NR3R4 (e.g. dimethylaminosulphonyl), —NR3SO2R4, —NR3SO2NR4R5, —NR3C(O)OR4, optionally substituted —C1-C4 alkyl (e.g. propyl, isobutyl or tert butyl), optionally substituted C1-C2 alkyl (e.g. methyl or eithyl), optionally substituted —C1-C6 alkoxy, optionally substituted —C2-C6 alkenyl, optionally substituted —C2-C6 alkynyl, a covalent bond, an oxygen atom, a sulphur atom, —SO—, —SO2—, —CO—, —C(O)O—, —CONR3—, —NR3— (e.g. methylamino), —NR3CO—, —NR3CONR4—, —SO2NR3—, —NR3SO2—, —NR3SO2NR4—, —NR3C(O)O—, —NR3C(O)OR4—, optionally substituted C1-C4 alkylene (e.g. methylene or ethylene) or optionally substituted —C2-C4 alkenylene (e.g. vinyl).
  • When n is 0, ring A may be substituted with one or more (e.g. one, two, three or four) Q1 substituents independently selected from halogen (e.g. fluorine, chlorine or bromine), cyano, oxo, nitro, —OR3, —SR3, —NR3R4, —CONR3R4, —NR3C(O)R4, —NR3C(O)NR4R5, —C(O)R3, —C(O)OR3, —SO2R3, —SO2NR3R4, —NR3SO2R4, —NR3SO2NR4R5, —NR3C(O)OR4, —C1-C6 alkyl, —C1-C6 alkoxy, —C2-C6 alkenyl, or —C2-C6 alkynyl, wherein alkyl, alkoxy, alkenyl or alkynyl, may be unsubstituted or substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF5, and wherein R3, R4 and R5 are as defined above.
  • In particular, when n is 0, Q1 may represent halogen (e.g. fluorine or chlorine), C1-C6 alkyl or C1-C3 alkyl optionally substituted with one or more fluorine, e.g. CF3.
  • In particular examples, n is 0 and ring A represents a 5 or 6 membered heteroaryl or aryl ring which is optionally substituted with one or more (e.g. one, two, three or four) Q1 substituents independently selected from halogen (e.g. fluorine or chlorine), C1-C6 alkyl or C1-C3 alkyl optionally substituted with one or more fluorine, e.g. CF3.
  • Alternatively, n is 0 and ring A represents a 9 or 10 membered heteroaryl or aryl ring which is optionally substituted with one or more (e.g. one, two, three or four) Q1 substituents independently selected from halogen (e.g. fluorine or chlorine), C1-C6 alkyl or C1-C3 alkyl optionally substituted with one or more fluorine, e.g. CF3.
  • When n is 1, Q1 is a covalent bond or a linker selected from covalent bond, an oxygen atom, a sulphur atom, —SO—, —SO2—, —CO—, —C(O)O—, —CONR3—, —NR3—, —NR3CO—, —NR3CONR4—, —SO2NR3—, —NR3SO2—, —NR3SO2NR4—, —NR3C(O)O—, —NR3C(O)OR4—, C1-C6 alkylene or —C2-C6 alkenylene, wherein the alkylene or alkenylene is optionally substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF5.
  • In particular, when n is 1, Q1 is a covalent bond, an oxygen atom, C1-C6 alkylene or C1-C3 alkylene, wherein the alkylene is optionally substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF5.
  • It is preferred that ring A is substituted with a further ring either directly or via a linker, i.e. ring A is substituted with at least one -Q1-(R2)n wherein n is 1. Substitution with a further ring is especially preferred when ring A is a monocycle.
  • In all cases described herein, R2 represents a 3 to 10 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring. R2 may be selected from cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, decahydronaphthalenyl, phenyl, naphthyl, naphthalenyl, pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, furyl, pyrrolyl, oxazolyl, thiazolyl, pyrazolyl, tetrazolyl, indolyl, indolizinyl, isoindolyl, indolinyl, purinyl, furazanyl, imidazolyl, indazolyl, isothiazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, thiadiazolyl, benzofuranyl, isobenzofuranyl, benzothiophenyl, isobenzothiophenyl, benzimidazolyl, benzothiazolyl, napthyridinyl, pteridinyl, pyrazinyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl, imidazopyridinyl, pyrazolopyridinyl, thiazolopyridinyl, isoindolinyl, triazinyl, dihydrophyridinyl, dihydropyrrolopyridinyl, quinoxalinyl, benzomorpholinyl, azetidinyl, pyrrolidinyl, piperidinyl, azepanyl, diazepanyl, dihydrofuranyl (e.g. 2,3-dihydrofuranyl, 2,5-dihydrofuranyl), dioxolanyl, morpholinyl, oxazolidinyl, oxazinanyl, indolinyl, isoindolinyl, piperazinyl, tetrahydrofuranyl, thiomorpholinyl, dihydropyranyl (e.g. 3,4-dihydropyranyl, 3,6-dihydropyranyl), homopiperazinyl, dioxanyl, hexahydropyrimidinyl, pyrazolinyl, pyrazolidinyl, 4H-quinolizinyl, quinuclidinyl, tetrahydropyranyl, tetrahydropyridinyl, tetrahydropyrimidinyl, tetrahydrothiophenyl, tetrahydropyridopyrazinyl, thiazolidinyl, benzopyranyl, tetrahydroquinolinyl, benzomorpholinyl and tetrahydroisoquinolinyl.
  • For example, R2 may be selected from cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, decahydronaphthalenyl, phenyl, naphthyl, naphthalenyl, pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, furyl, pyrrolyl, oxazolyl, thiazolyl, pyrazolyl, tetrazolyl, indolyl, indolizinyl, isoindolyl, indolinyl, purinyl, furazanyl, imidazolyl, indazolyl, isothiazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, thiadiazolyl, benzofuranyl, isobenzofuranyl, benzothiophenyl, isobenzothiophenyl, benzimidazolyl, benzothiazolyl, napthyridinyl, pteridinyl, pyrazinyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl, imidazopyridinyl, pyrazolopyridinyl, thiazolopyridinyl, isoindolinyl, triazinyl, dihydrophyridinyl, quinoxalinyl, benzomorpholinyl, azetidinyl, pyrrolidinyl, piperidinyl, azepanyl, diazepanyl, dihydrofuranyl (e.g. 2,3-dihydrofuranyl, 2,5-dihydrofuranyl), dioxolanyl, morpholinyl, oxazolidinyl, oxazinanyl, indolinyl, isoindolinyl, piperazinyl, tetrahydrofuranyl, thiomorpholinyl, dihydropyranyl (e.g. 3,4-dihydropyranyl, 3,6-dihydropyranyl), homopiperazinyl, dioxanyl, hexahydropyrimidinyl, pyrazolinyl, pyrazolidinyl, 4H-quinolizinyl, quinuclidinyl, tetrahydropyranyl, tetrahydropyridinyl, tetrahydropyrimidinyl, tetrahydrothiophenyl, thiazolidinyl, benzopyranyl, tetrahydroquinolinyl, benzomorpholinyl and tetrahydroisoquinolinyl.
  • R2 may represent an optionally substituted 5 or 6 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring.
  • Alternatively, R2 may represent an optionally substituted 9 or 10 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring.
  • In particular, R2 is selected from substituted or unsubstituted phenyl, pyrazolyl, indazolyl, imidazolyl and thiazolyl. More particularly, R2 is phenyl.
  • In all cases described herein, R2 may be optionally substituted with one or more substituents selected from halogen, cyano, oxo, nitro, —OR6, —SR6, —NR6R7, —CONR6R7, —NR6COR7, —NR6CONR7R8, —COR6, —C(O)OR6, —SO2R6, —SO2NR6R7, —NR6SO2R7, —NR6SO2NR7R8, —NR6C(O)OR7, optionally substituted —C1-C6 alkyl, optionally substituted —C1-C6 alkoxy, optionally substituted —C2-C6 alkenyl, optionally substituted —C2-C6 alkynyl, -Q2-R6, -Q2-NR6CONR7R8, -Q2-NR6R7, -Q2-COR6, -Q2-NR6COR6, -Q2-NR6C(O)OR7, -Q2-SO2R6, Q2-CONR6R7, -Q2-CO2R6, -Q2-SO2NR6R7, -Q2-NR6SO2R7 and -Q2-NR6SO2NR7R8, wherein the alkyl, alkoxy, alkenyl or alkynyl are optionally substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF5; wherein
  • Q2 represents a covalent bond, an oxygen atom, a sulphur atom, —SO—, —SO2—, —CO—, optionally substituted C1-C6 alkylene or optionally substituted C2-C6 alkenylene; and
  • R6, R7, R8 each independently represent hydrogen, optionally substituted C1-C6 alkyl, optionally substituted heterocyclyl, optionally substituted heteroaryl, optionally substituted aryl, or an optionally substituted cycloalkyl.
  • R2 may be substituted with one or more (e.g. one, two, three or four), in particular one or two, substituents independently selected from halogen, cyano, oxo, nitro, —OR6, —SR6, —NR6R7, —CONR6R7, —NR6COR7, —NR6CONR7R8, —COR6, —C(O)OR6, —SO2R6, —SO2NR6R7, —NR6SO2R7, —NR6SO2NR7R8, —NR6C(O)OR7, optionally substituted —C1-C6 alkyl, optionally substituted —C1-C6 alkoxy, optionally substituted —C2-C6 alkenyl, optionally substituted —C2-C6 alkynyl, -Q2-R6, -Q2-NR6CONR7R8, -Q2-NR6R7, -Q2-COR6, -Q2-NR6COR7, -Q2-NR6C(O)OR7, -Q2-SO2R6, -Q2-CONR6R7, -Q2-CO2R6, -Q2-SO2NR6R7, -Q2-NR6SO2R7 and -Q2-NR6SO2NR7R8, wherein Q2 represents a covalent bond, an oxygen atom, a sulphur atom, —SO—, —SO2—, —CO—, C1-C6 alkylene or optionally substituted C2-C6 alkenylene, and wherein R6, R7, R8 each independently represent hydrogen or optionally substituted C1-C6 alkyl, wherein any alkyl, alkoxy, alkenyl, alkynyl, alkylene or alkenylene is optionally substituted with one or more (e.g. one, two, three or four) substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF5.
  • In particular, R2 may be substituted with one or more substituents selected from cyano, C(O)NR6R7, —C1-C4 alkyl (e.g. propyl, isobutyl or tert butyl) or C1-C2 alkyl (e.g. methyl or ethyl), and a 3 to 10 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring, wherein R6 and R7 each independently represent hydrogen or optionally substituted C1-C6 alkyl. The alkyl may be optionally substituted with one or more fluorine.
  • More particularly, R2 may be mono-substituted with a substituent selected from cyano, C(O)NR6R7, —C1-C3 alkyl, in particular methyl, and imidazolyl, wherein R6 and R7 each independently represent hydrogen or methyl.
  • In addition, or alternatively, R2 may be optionally substituted with a further optionally substituted 3 to 10 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring, either directly attached or via a linking group. The linking group may be an oxygen atom, a carbonyl or an optionally substituted C1-C6 alkylene. The linking group may be oxygen, —CO— or an alkylene chain, for example, methylene. The 3 to 10 membered ring may be unsubstituted or substituted with one or more (e.g. one, two, three of four), in particular one or two, substituents selected from halogen (for example, fluorine or chlorine), C1-C4 alkyl (e.g. propyl, isobutyl or tert butyl) or C1-C2 alkyl (e.g. methyl or ethyl) wherein the alkyl may be optionally substituted with one or more fluorine. In particular, the 3 to 10 membered ring is unsubstituted.
  • In particular, R2 may be unsubstituted, mono-substituted or di-substituted. More particularly, R2 is unsubstituted or mono-substituted.
  • In certain instances, R2 represents a 3 to 10 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring selected from heterocyclyl, cycloalkyl, heteroaryl or aryl ring selected from cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, decahydronaphthalenyl, phenyl, naphthyl, naphthalenyl, pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, furyl, pyrrolyl, oxazolyl, thiazolyl, pyrazolyl, tetrazolyl, indolyl, indolizinyl, isoindolyl, indolinyl, purinyl, furazanyl, imidazolyl, indazolyl, isothiazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, thiadiazolyl, benzofuranyl, isobenzofuranyl, benzothiophenyl, isobenzothiophenyl, benzimidazolyl, benzothiazolyl, napthyridinyl, pteridinyl, pyrazinyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl, imidazopyridinyl, pyrazolopyridinyl, thiazolopyridinyl, isoindolinyl, triazinyl, dihydrophyridinyl, quinoxalinyl, benzomorpholinyl, azetidinyl, pyrrolidinyl, piperidinyl, azepanyl, diazepanyl, dihydrofuranyl (e.g. 2,3-dihydrofuranyl, 2,5-dihydrofuranyl), dioxolanyl, morpholinyl, oxazolidinyl, oxazinanyl, indolinyl, isoindolinyl, piperazinyl, tetrahydrofuranyl, thiomorpholinyl, dihydropyranyl (e.g. 3,4-dihydropyranyl, 3,6-dihydropyranyl), homopiperazinyl, dioxanyl, hexahydropyrimidinyl, pyrazolinyl, pyrazolidinyl, 4H-quinolizinyl, quinuclidinyl, tetrahydropyranyl, tetrahydropyridinyl, tetrahydropyrimidinyl, tetrahydrothiophenyl, thiazolidinyl, benzopyranyl, tetrahydroquinolinyl, benzomorpholinyl and tetrahydroisoquinolinyl which is either unsubstituted or substituted with one or more (e.g. one, two or three) substituents selected from halogen (e.g. fluorine or chlorine), cyano, oxo, nitro, —OR6, —SR6, —NR6R7, —CONR6R7, —NR6COR7, —NR6CONR7R8, —COR6, —C(O)OR6, —SO2R6, —SO2NR6R7, —NR6SO2R7, —NR6SO2NR7R8, —NR6C(O)OR7, optionally substituted —C1-C6 alkyl, optionally substituted —C1-C6 alkoxy, optionally substituted —C2-C6 alkenyl, optionally substituted —C2-C6 alkynyl, -Q2-R6, -Q2-NR6CONR7R8, -Q2-NR6R7, -Q2-COR6, -Q2-NR6COR6, -Q2-NR6C(O)OR7, -Q2-SO2R6, Q2-CONR6R7, -Q2-CO2R6, -Q2-SO2NR6R7, -Q2-NR6SO2R7 and -Q2-NR6SO2NR7R8, wherein the alkyl, alkoxy, alkenyl or alkynyl are optionally substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF5, wherein Q2 represents a covalent bond, an oxygen atom, a sulphur atom, —SO—, —SO2—, —CO—, C1-C6 alkylene or optionally substituted C2-C6 alkenylene, and R6, R7, R8 each independently represent hydrogen, optionally substituted C1-C6 alkyl, optionally substituted heterocyclyl, optionally substituted heteroaryl, optionally substituted aryl, or an optionally substituted cycloalkyl.
  • R2 may represent a ring selected from phenyl, pyrazolyl, indazolyl, imidazolyl and thiazolyl, wherein the ring is unsubstituted or substituted with one or more, in particular one or two, substituents selected from halogen (e.g. fluorine or chlorine), cyano, oxo, nitro, —OR6, —SR6, —NR6R7, —CONR6R7, —NR6COR7, —NR6CONR7R8, —COR6, —C(O)OR6, —SO2R6, —SO2NR6R7, —NR6SO2R7, —NR6SO2NR7R8, —NR6C(O)OR7, optionally substituted —C1-C6 alkyl, optionally substituted —C1-C6 alkoxy, optionally substituted —C2-C6 alkenyl, optionally substituted —C2-C6 alkynyl, -Q2-R6, -Q2-NR6CONR7R8, -Q2_NR6R7, -Q2-COR6, -Q2-NR6COR7, -Q2-NR6C(O)OR7, -Q2-SO2R6, Q2-CONR6R7, -Q2-CO2R6, -Q2-SO2NR6R7, -Q2-NR6SO2R7 and -Q2-NR6SO2NR7R8, wherein the alkyl, alkoxy, alkenyl or alkynyl are optionally substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF5, wherein Q2 represents a covalent bond, an oxygen atom, a sulphur atom, —SO—, —SO2—, —CO—, C1-C6 alkylene or optionally substituted C2-C6 alkenylene, and R6, R7, R8 each independently represent hydrogen, optionally substituted C1-C6 alkyl, optionally substituted heterocyclyl, optionally substituted heteroaryl, optionally substituted aryl, or an optionally substituted cycloalkyl.
  • R2 may represent a ring selected from cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, decahydronaphthalenyl, phenyl, naphthyl, naphthalenyl, pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, furyl, pyrrolyl, oxazolyl, thiazolyl, pyrazolyl, tetrazolyl, indolyl, indolizinyl, isoindolyl, indolinyl, purinyl, furazanyl, imidazolyl, indazolyl, isothiazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, thiadiazolyl, benzofuranyl, isobenzofuranyl, benzothiophenyl, isobenzothiophenyl, benzimidazolyl, benzothiazolyl, napthyridinyl, pteridinyl, pyrazinyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl, imidazopyridinyl, pyrazolopyridinyl, thiazolopyridinyl, isoindolinyl, triazinyl, dihydrophyridinyl, quinoxalinyl, benzomorpholinyl, azetidinyl, pyrrolidinyl, piperidinyl, azepanyl, diazepanyl, dihydrofuranyl (e.g. 2,3-dihydrofuranyl, 2,5-dihydrofuranyl), dioxolanyl, morpholinyl, oxazolidinyl, oxazinanyl, indolinyl, isoindolinyl, piperazinyl, tetrahydrofuranyl, thiomorpholinyl, dihydropyranyl (e.g. 3,4-dihydropyranyl, 3,6-dihydropyranyl), homopiperazinyl, dioxanyl, hexahydropyrimidinyl, pyrazolinyl, pyrazolidinyl, 4H-quinolizinyl, quinuclidinyl, tetrahydropyranyl, tetrahydropyridinyl, tetrahydropyrimidinyl, tetrahydrothiophenyl, thiazolidinyl, benzopyranyl, tetrahydroquinolinyl, benzomorpholinyl and tetrahydroisoquinolinyl, wherein the ring is unsubstituted or substituted with cyano, C(O)NR6R7, —C1-C4 alkyl (e.g. propyl, isobutyl or tert butyl) or C1-C2 alkyl (e.g. methyl or ethyl), and a 3 to 10 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring, wherein R6 and R7 each independently represent hydrogen or optionally substituted C1-C6 alkyl. The alkyl may be optionally substituted with one or more fluorine.
  • In particular, R2 may be selected from phenyl, pyrazolyl, indazolyl, imidazolyl and thiazolyl wherein the ring is unsubstituted or substituted with one or more (e.g. one, two or three) substitutents selected from cyano, C(O)NR6R7, —C1-C6 alkyl, and a 3 to 10 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring, wherein R6 and R7 each independently represent hydrogen or optionally substituted C1-C6 alkyl.
  • The present invention further relates to compounds of formula (I), or a pharmaceutically acceptable salt thereof, wherein:
  • R1a, R1b, R1e and R1d each independently represent hydrogen or C1-C3 alkyl which may be optionally substituted with one or more fluorine;
  • R1e and R1f independently represent hydrogen, fluorine, C1-C3 alkyl or C1-C3 alkoxy, wherein the alkyl or alkoxy may be optionally substituted with one or more fluorine;
  • A represents a 5 to 10 membered monocyclic or bicyclic heteroaryl or aryl ring which is unsubstituted or substituted with one, two or three of -Q1-(R2)n;
  • n is 0 or 1;
  • Q1, R2 and n are as defined herein.
  • In particular, Q1 is selected from halogen (e.g. fluorine, chlorine or bromine), cyano, oxo, nitro, —OR3 (e.g hydroxyl), —SR3 (e.g. thiol), —NR3R4 (e.g. amino or N,N-dimethylamino), —CONR3R4 (e.g. amido), —NR3COR4 (N-acetyl), —NR3CONR4R5, —COR3 (e.g. acetyl), —C(O)OR3 (e.g. methoxycarbonyl or ethoxycarbonyl), —SO2R3 (e.g. methyl sulphonyl), —SO2NR3R4 (e.g. dimethylaminosulphonyl), —NR3SO2R4, —NR3SO2NR4R5, —NR3C(O)OR4, optionally substituted —C1-C4 alkyl (e.g. propyl, isobutyl or tert butyl), optionally substituted C1-C2 alkyl (e.g. methyl or eithyl), optionally substituted —C1-C6 alkoxy, optionally substituted —C2-C6 alkenyl, optionally substituted —C2-C6 alkynyl, a covalent bond, an oxygen atom, a sulphur atom, —SO—, —SO2—, —CO—, —C(O)O—, —CONR3—, —NR3— (e.g. methylamino), —NR3CO—, —NR3CONR4—, —SO2NR3—, —NR3SO2—, —NR3SO2NR4—, —NR3C(O)O—, —NR3C(O)OR4—, optionally substituted C1-C4 alkylene (e.g. methylene or ethylene) or optionally substituted —C2-C4 alkenylene (e.g. vinyl), and R2 is a 5 or 6 membered heteroaryl, heterocyclyl or aryl ring optionally substituted with one or two substituents independently selected from halogen, cyano, oxo, nitro, —OR6, —SR6, —NR6R7, —CONR6R7, —NR6COR7, —NR6CONR7R8, —COR6, —C(O)OR6, —SO2R6, —SO2NR6R7, —NR6SO2R7, —NR6SO2NR7R8, —NR6C(O)OR7, optionally substituted —C1-C6 alkyl, optionally substituted —C1-C6 alkoxy, optionally substituted —C2-C6 alkenyl, optionally substituted —C2-C6 alkynyl, -Q2-R6, -Q2-NR6CONR7R8, -Q2-NR6R7, -Q2-COR6, -Q2-NR6COR7, -Q2-NR6C(O)OR7, -Q2-SO2R6, Q2_CONR6R7, -Q2-CO2R6, -Q2-SO2NR6R7, -Q2-NR6SO2R7 and -Q2-NR6SO2NR7R8, wherein Q2 represents a covalent bond, an oxygen atom, a sulphur atom, —SO—, —SO2—, —CO—, C1-C6 alkylene or optionally substituted C2-C6 alkenylene, and wherein R6, R7, R8 each independently represent hydrogen or optionally substituted C1-C6 alkyl, wherein any alkyl, alkoxy, alkenyl, alkynyl, alkylene or alkenylene is optionally substituted with one or more (e.g. one, two, three or four) substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF5.
  • The present invention further relates to compounds of formula (I), or a pharmaceutically acceptable salt thereof, wherein:
  • R1a, R1b, R1c and R1d are each hydrogen;
  • A represents a 5 to 10 membered monocyclic or bicyclic heteroaryl or aryl ring which is unsubstituted or substituted with one or two of -Q1-(R2)n;
  • each occurrence of -Q1-(R2)n is the same or different, wherein:
  • Q1 represents halogen (e.g. fluorine or chlorine), C1-C6 alkyl or C1-C3 alkyl optionally substituted with one or more fluorine, a covalent bond, an oxygen atom, C1-C6 alkylene or C1-C3 alkylene, wherein the alkylene is optionally substituted with one or more substitutents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF5;
  • R2 represents a 5 to 10 membered heterocyclyl, cycloalkyl, heteroaryl or aryl ring, in particular, R2 represents phenyl, pyrazolyl, indazolyl, imidazolyl and thiazolyl.
  • Examples of the heteroaryl and aryl ring represented by A include those shown below:
  • Figure US20180362460A1-20181220-C00006
  • wherein
  • Figure US20180362460A1-20181220-C00007
  • represents the point of attachment to the remainder of the molecule, i.e. to the amide nitrogen, and wherein ring A is optionally substituted with one or more of -Q1-(R2)n. Hydrogen atoms attached to the ring nitrogen atoms have not been shown. It will be understood by the skilled person which ring nitrogen atoms are suitable for substitution and where not substituted the nitrogen may be bound to a hydrogen atom to complete its valency, where appropriate.
  • Examples of novel compounds of formula (I) include:
    • N-(4-chloro-3-(trifluoromethyl)phenyl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
    • 1-cyano-3-fluoro-N-(4-phenylthiazol-2-yl)pyrrolidine-3-carboxamide
    • N-(benzo[d]thiazol-6-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
    • 1-cyano-3-fluoro-N-(quinolin-3-yl)pyrrolidine-3-carboxamide
    • 1-cyano-3-fluoro-N-(quinolin-6-yl)pyrrolidine-3-carboxamide
    • 1-cyano-3-fluoro-N-(3-(2-methylthiazol-4-yl)phenyl)pyrrolidine-3-carboxamide
    • 1-cyano-3-fluoro-N-(3-phenoxyphenyl)pyrrolidine-3-carboxamide
    • 1-cyano-3-fluoro-N-(5-phenylthiazol-2-yl)pyrrolidine-3-carboxamide
    • (R)-1-cyano-3-fluoro-N-(5-phenylthiazol-2-yl)pyrrolidine-3-carboxamide
    • 1-cyano-3-fluoro-N-(5-phenylisoxazol-3-yl)pyrrolidine-3-carboxamide
    • 1-cyano-3-fluoro-N-(1-phenyl-1H-imidazol-4-yl)pyrrolidine-3-carboxamide
    • (S)-1-cyano-3-fluoro-N-(1-phenyl-1H-pyrazol-4-yl)pyrrolidine-3-carboxamide
    • (R)-1-cyano-3-fluoro-N-(1-phenyl-1H-pyrazol-4-yl)pyrrolidine-3-carboxamide
    • (R)-1-cyano-N-(1-(4-cyanophenyl)-1H-imidazol-4-yl)-3-fluoropyrrolidine-3-carboxamide
    • (R)—N-(1-benzyl-1H-pyrazol-4-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
    • N-(6-(1H-pyrazol-4-yl)benzo[d]thiazol-2-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
    • 1-cyano-3-fluoro-N-(6-phenylbenzo[d]thiazol-2-yl)pyrrolidine-3-carboxamide
    • N-(5-(1H-indazol-4-yl)thiazol-2-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
    • (R)—N-(5-(1H-indazol-7-yl)thiazol-2-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
    • 1-cyano-3-fluoro-N-(3-phenylisoxazol-5-yl)pyrrolidine-3-carboxamide
    • (R)-1-cyano-3-fluoro-N-(3-phenylisoxazol-5-yl)pyrrolidine-3-carboxamide
    • N-(5-(3-carbamoylphenyl)thiazol-2-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
    • 1-cyano-3-fluoro-N-(5-(3-(methylcarbamoyl)phenyl)thiazol-2-yl)pyrrolidine-3-carboxamide
    • (R)-1-cyano-3-fluoro-N-(5-(3-(methylcarbamoyl)phenyl)thiazol-2-yl)pyrrolidine-3-carboxamide
    • N-(5-(3-(1H-imidazol-1-yl)phenyl)thiazol-2-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
    • N-(3-(3-(1H-imidazol-1-yl)phenyl)isoxazol-5-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
    • (R)—N-(3-(3-(1H-imidazol-1-yl)phenyl)isoxazol-5-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
    • N-(6-(1H-pyrazol-5-yl)imidazo[1,2-a]pyridin-2-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
    • 1-cyano-3-fluoro-N-(6-(3-(methylcarbamoyl)phenyl)benzo[d]thiazol-2-yl)pyrrolidine-3-carboxamide
    • or pharmaceutically acceptable salts thereof.
  • It should be noted that each of the chemical compounds listed above represents a particular and independent aspect of the invention.
  • According to a further aspect of the invention there is provided a process for the preparation of a compound of formula (I) or a pharmaceutically acceptable salt thereof comprising the steps of reacting an acid of formula (III) with a compound A-NH2 to form an amide:
  • Figure US20180362460A1-20181220-C00008
  • Where R1a-R1f are as defined elsewhere and PG is an amine protecting group. The protecting group may be but is not limited to BOC. It is clear to a person skilled in the art to combine or adjust such a protecting chemical group. After coupling of A-NH2 to form an amide, the protecting group may be removed to leave the free amine according to formula (IV) which can then be treated with cyanogen bromide to form compounds according to formula (I).
  • According to a further aspect of the invention there is provided a process for the preparation of a compound of formula (I) or a pharmaceutically acceptable salt thereof comprising the steps of reacting an amine of formula (IV) with cyanogen bromide to form N—CN compounds:
  • Figure US20180362460A1-20181220-C00009
  • Where R1a-R1f and A are as defined elsewhere.
  • According to a further aspect of the invention there is provided a pharmaceutical composition comprising a compound of the invention.
  • Pharmaceutical compositions of this invention comprise any of the compounds of the invention combined with any pharmaceutically acceptable carrier, adjuvant or vehicle.
  • Examples of pharmaceutically acceptable carriers, are known to those skilled in the art and include but are not limited to preserving agents, fillers, disintegrating agents, wetting agents, emulsifying agents, suspending agents, sweetening agents, flavouring agents, perfuming agents, antibacterial agents, antifungal agents, lubricating agents and dispersing agents, depending on the nature of the mode of administration and dosage forms. The compositions may be in the form of, for example, tablets, capsules, powders, granules, elixirs, lozenges, suppositories, syrups and liquid preparations including suspensions and solutions. The term “pharmaceutical composition” in the context of this invention means a composition comprising an active agent and comprising additionally one or more pharmaceutically acceptable carriers. The composition may further contain ingredients selected from, for example, diluents, adjuvants, excipients, vehicles, preserving agents, fillers, disintegrating agents, wetting agents, emulsifying agents, suspending agents, sweetening agents, flavouring agents, perfuming agents, antibacterial agents, antifungal agents, lubricating agents and dispersing agents, depending on the nature of the mode of administration and dosage forms.
  • The compounds of the invention may be used in the treatment of disorders and diseases related to DUB inhibition, particularly Cezanne 1 and USP30 inhibition.
  • According to a further aspect of the invention there is provided a compound of formula (I) or pharmaceutical composition thereof for use in therapy. In particular, the compounds of the invention have use in the treatment of cancer and more particularly in the treatment of cancers linked to DUB activity. Compounds of the invention may be useful against any DUB enzyme, including but not limited to Cezanne 1 and USP30.
  • The compounds described herein may be used in the manufacture of a medicament for the treatment of cancer linked to DUB activity.
  • In a further aspect of the invention there is provided a method of treatment or prevention of cancer linked to Cezanne 1 or USP30 activity, the method comprising administering a pharmaceutically effective amount of a compound of the invention or a pharmaceutical composition thereof to an individual suffering from a cancer linked to Cezanne 1 or USP30 activity.
  • The compounds or compositions disclosed herein may be used to treat cancer. References to “cancer” or “tumour” include but are not limited to breast, ovarian, prostate, lung, kidney, gastric, colon, testicular, head and neck, pancreas, brain, melanoma, bone or other cancers of tissue organs and cancers of the blood cells such as lymphomas and leukaemias. Particular cancers include lymphoma, multiple myeloma, colorectal cancer, and non-small cell lung carcinoma.
  • The compounds or compositions disclosed herein may be used to treat additional diseases linked to Cezanne 1 activity.
  • The compounds of the invention or pharmaceutical compositions thereof as described herein may be combined with one or more additional agents. The compounds may be combined with one or more additional anti-tumour therapeutic agents, for example chemotherapeutic drugs or inhibitors of other regulatory proteins. In one embodiment the one or more anti-tumour therapeutic agent is selected from a PARP (poly ADP ribose polymerase) inhibitor, a BRCA2 inhibitor and an ATM inhibitor. In another embodiment the PARP (poly ADP ribose polymerase) inhibitor is an inhibitory RNA (RNAi) molecule (PARPi). In a further embodiment PARP inhibitors may be selected from one or more of Iniparib (BSI 201), Olaparib (AZD-2281), Rucaparib (AG014699, PF-01367338) and Veliparib (ABT-888), MK-4827, CEP-9722, E7016(GPI-21016), LT-673, MP-124, NMS-P118. In a further embodiment the one or more anti-tumour agent is a chemotherapeutic agent. Chemotherapeutic agents may be selected from olaparib, mitomycin C, cisplatin, carboplatin, oxaliplatin, ionizing radiation (IR), camptothecin, irinotecan, topotecan, temozolomide, taxanes, 5-fluoropyrimidines, gemcitabine, and doxorubicin.
  • As discussed above, the compounds of the invention may be useful in the treatment of disorders and diseases related to USP30 inhibition. The compounds of the invention may therefore be useful in the treatment of disorders or diseases having a component relating to mitochondiral dysfunction.
  • Mitochondrial dysfunctions result from defects of the mitochondria, which are specialized compartments present in every cell of the body except red blood cells. When mitochondria fail, less and less energy is generated within the cell and cell injury or even cell death will follow. If this process is repeated throughout the body the life of the subject in whom this is happening is severely compromised. Diseases of the mitochondria appear most often in organs that are very energy demanding such as the brain, heart, liver, skeletal muscles, kidney and the endocrine and respiratory system.
  • The condition involving mitochondrial dysfunction may be selected from a condition involving a mitophagy defect, a condition involving a mutation in mitochondrial DNA, a condition involving mitochondrial oxidative stress, a condition involving a defect in mitochondrial membrane potential, mitochondrial biogenesis, a condition involving a defect in mitochondrial shape or morphology, and a condition involving a lysosomal storage defect.
  • In particular, the condition involving mitochondrial dysfunction may be selected from a neurodegenerative disease; multiple sclerosis (MS), mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome; Leber's hereditary optic neuropathy (LHON); cancer; neuropathy, ataxia, retinitis pigmentosa-maternally inherited Leigh syndrome (NARP-MILS); Danon disease; diabetes; diabetic nephropathy; metabolic disorders; heart failure; ischemic heart disease leading to myocardial infarction; psychiatric diseases, for example schizophrenia; multiple sulfatase deficiency (MSD); mucolipidosis II (ML II); mucolipidosis III (ML III); mucolipidosis IV (ML IV); GMl-gangliosidosis (GM1); neuronal ceroid-lipofuscinoses (NCL1); Alpers disease; Barth syndrome; Beta-oxidation defects; carnitine-acyl-carnitine deficiency; carnitine deficiency; creatine deficiency syndromes; co-enzyme Q10 deficiency; complex I deficiency; complex II deficiency; complex III deficiency; complex IV deficiency; complex V deficiency; COX deficiency; chronic progressive external ophthalmoplegia syndrome (CPEO); CPT I deficiency; CPT II deficiency; glutaric aciduria type II; Kearns-Sayre syndrome; lactic acidosis; long-chain acyl-CoA dehydrogenase deficiency (LCHAD); Leigh disease or syndrome; lethal infantile cardiomyopathy (LIC); Luft disease; glutaric aciduria type II; medium-chain acyl-CoA dehydrogenase deficiency (MCAD); myoclonic epilepsy and ragged-red fiber (MERRF) syndrome; mitochondrial cytopathy; mitochondrial recessive ataxia syndrome; mitochondrial DNA depletion syndrome; myoneurogastointestinal disorder and encephalopathy; Pearson syndrome; pyruvate dehydrogenase deficiency; pyruvate carboxylase deficiency; POLG mutations; medium/short-chain 3-hydroxyacyl-CoA dehydrogenase (M/SCHAD) deficiency; very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency; and age-dependent decline in cognitive function and muscle strength.
  • The condition involving mitochondrial dysfunction may be a CNS disorder, for example a neurodegenerative disease. Neurodegenerative diseases include, but are not limited to, Parkinson's disease, Alzheimer's disease, amyotrophic lateral sclerosis (ALS), Huntington's disease, ischemia, stroke, dementia with Lewy bodies, and frontotemporal dementia.
  • In one embodiment, the condition involving mitochondrial dysfunction is a CNS disorder.
  • Dosage Forms
  • The pharmaceutical compositions of the invention may be designed for administration by the oral, parenteral or mucosal route and the choice or the specific form of composition is dependent on the administration route. Thus for oral administration the composition may be in the form, for example, of tablets, lozenges, dragees, films, powders, elixirs, syrups, liquid preparations including dispersions, suspensions, emulsions, solutions or sprays, cachets, granules, capsules, etc. For administration to mucosa the composition may be in the form of sprays, inhalants, dispersions, suspensions, emulsions, solutions, gels, patches, films, ointments, creams, lotions, suppositories etc. For parenteral administration the composition is in the form of a liquid preparation such as a solution, dispersion, emulsion or suspension including liposome compositions.
  • Preparations according to the invention for parenteral administration include sterile aqueous, aqueous-organic, and organic solutions, suspensions and emulsions.
  • Such dosage forms are prepared according to techniques known in the art of pharmaceutical formulation. When in the form of sprays or inhalants the pharmaceutical compositions may be administered nasally. Suitable formulations for this purpose are known to those skilled in the art.
  • The pharmaceutical compositions of the invention may be administered by injection and may be in the form of a sterile liquid preparation for injection, including liposome preparations. The pharmaceutical compositions of the invention may also be in the form of suppositories for rectal administration.
  • These are formulated so that the pharmaceutical composition is solid at room temperature and liquid at body temperature to allow release of the active compound.
  • The dosages may be varied depending upon the requirements of the patient, the severity of the condition being treated, and the compound being employed. Determination of the proper dosage for a particular situation is within the remit of the person skilled in the skill of the art. Generally, treatment is initiated with smaller dosages which are less than the optimal dose of the compound. Thereafter the dosage is increased by small increments until the optimum effect under the circumstances is reached.
  • The magnitude of an effective dose of a compound will, of course, vary with the nature of the severity of the condition to be treated and with the particular compound and its route of administration. The selection of appropriate dosages is within the ability of one of ordinary skill in this art, without undue burden. The daily dose range is about 10 μg to about 100 mg per kg body weight of a human and non-human animal and in general may be around 10 μg to 30 mg per kg body weight per dose. The above dose may be given from one to three times per day.
  • Synthetic Methodologies
  • Compounds of the invention may be prepared via a variety of synthetic routes. Exemplary routes to certain compounds of the invention are shown below. Representative compounds of the present invention can be synthesized in accordance with the general synthetic methods described below and are illustrated more particularly in the schemes that follow. Since the schemes are an illustration, the invention should not be construed as being limited by the chemical reactions and conditions expressed. The preparation of the various starting materials used in the schemes is well within the skill of persons versed in the art. Those skilled in the art appreciate that, where appropriate, the individual transformations within a scheme can be completed in a different order. The following schemes describe general synthetic methods whereby intermediate and target compounds of the present invention may be prepared. Additional representative compounds and stereoisomers, racemic mixtures, diastereomers and enantiomers thereof can be synthesized using the intermediates prepared in accordance to the general schemes and other materials, compounds and reagents known to those skilled in the art. All such compounds, stereoisomers, racemic mixtures, diastereomers and enantiomers thereof are intended to be encompassed within the scope of the present invention.
  • All the compounds were characterised by liquid chromatography-mass spectroscopy (LCMS) and 1H NMR.
    • Synthetic Schemes Abbreviations
  • BOC Tert-butoxycarbonyl
  • br Broad (NMR signal)
  • d Doublet (NMR signal)
  • DCM Dichloromethane
  • DIAD Diisopropyl azodicarboxylate
  • DIPEA Diisopropylethyl amine
  • DMAP 4-methylaminopyridine
  • DMF N,N-Dimethylformamide
  • DMSO Dimethylsulphoxide
  • dppf 1,1′-Bis(diphenylphosphino)ferrocene
  • ES Electrospray
  • EtOAc Ethyl acetate
  • h Hour(s)
  • HATU 1-[Bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium3-oxid hexafluorophosphate
  • HBTU 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate
  • HPLC High performance liquid chromatography
  • LCMS Liquid chromatography-mass spectrometry
  • m Multiplet (NMR signal)
  • MeCN Acetonitrile
  • MeOH Methanol
  • Prep Preparative
  • rt Room temperature
  • s Singlet (NMR signal)
  • t Triplet (NMR signal)
  • TEA Triethylamine
  • TFA Trifluoroacetic acid
  • THF Tetrahydrofuran
  • TLC Thin layer chromatography
  • LCMS Methods
  • Method A
    Column XBridge ShieldRP18, 50*2.1 mm 5 μm or equivalent
    Mobile (A) 0.05% Ammonia in Water
    Phase (B) Acetonitrile
    Flow Rate 0.8 mL/min
    Gradient Time % B
    0.0 15
    0.4 15
    3.4 100
    4.0 100
    4.01 15
  • Method B
    Column Agilent TC-C18, 50 × 2.1 mm, 5 μm
    Mobile (A) 0.04% TFA in Water
    Phase (B) 0.02% TFA in Acetonitrile
    Flow Rate 0.8 mL/min
    Gradient Time % B
    0 0
    0.4 1
    3.4 100
    4 100
    Temperature 50° C.
  • Method C
    Column BEH C18, 50 × 2.1 mm, 1.7 μm or equivalent
    Mobile (A) 5 mM Ammonium Acetate + 0.1% Formic Acid in Water
    Phase (B) 0.1% Formic Acid in Acetonitrile
    Flow Rate 0.55 mL/min
    Gradient Time % B
    0.01 5
    0.40 5
    0.80 35
    1.20 55
    2.50 100
    3.30 100
    3.31 5
    4.00 5
  • Method D
    Column BEH C18, 50 × 2.1 mm, 1.7 μm or equivalent
    Mobile (A) 5 mM Ammonium Acetate + 0.1% Formic Acid in Water
    Phase (B) 0.1% Formic Acid in Acetonitrile
    Flow Rate 0.45 mL/min
    Gradient Time % B
    0.01 2
    0.50 2
    5.00 90
    6.00 95
    7.00 95
    7.01 2
    8.00 2
  • Method E
    Column X-bridge C18, 50 × 4.6 mm, 3.5 μm or equivalent
    Mobile (A) 0.1% Ammonia in Water
    Phase (B) 0.1% Ammonia in Acetonitrile
    Flow Rate 1.0 mL/min
    Gradient Time % B
    0.01 5
    5.00 90
    5.80 95
    7.20 95
    7.21 5
    10.00 5
  • Method F
    Column X-Bridge C18, 50 × 4.6 mm, 3.5 μm or equivalent
    Mobile (A) 0.1% Ammonia in Water
    Phase (B) 0.1% Ammonia in Acetonitrile
    Flow Rate
    1 mL/min
    Gradient Time % B
    0.01 0
    0.10 0
    2.50 90
    2.80 95
    3.60 95
    3.61 0
    5.00 0
  • Figure US20180362460A1-20181220-C00010
    • Example 1 N-(4-chloro-3-(trifluoromethyl)phenyl)-1-cyano-3-fluoropyrrolidine-3-carboxamide (Prepared According to General Scheme 1)
  • Figure US20180362460A1-20181220-C00011
  • Step a.
  • To a solution of 1-(tert-butoxycarbonyl)-3-fluoropyrrolidine-3-carboxylic acid (made according to WO2013020062 A1) (0.2 mmol) in DCM (1 mL) was added HATU (0.2 mmol). The reaction mixture was stirred at 0° C. for 20 min. The reaction mixture was treated with 4-chloro-3-(trifluoromethyl)aniline (0.2 mmol) and DIPEA (0.6 mmol) and stirred at rt for 16 h. The resulting mixture was concentrated under reduced pressure. The resulting residue was purified by prep-TLC (Petrol Ether/EtOAc=1:2) yielding tert-butyl 3-((4-chloro-3-(trifluoromethyl)phenyl)carbamoyl)-3-fluoropyrrolidine-1-carboxylate. LCMS: Method A, MS: ES+ 411.7.
  • Step b.
  • To a solution of tert-butyl 3-((4-chloro-3-(trifluoromethyl)phenyl)carbamoyl)-3-fluoropyrrolidine-1-carboxylate in EtOAc (1 mL) was added HCl/EtOAc (4M, 1 mL). The reaction mixture was stirred at rt for 2 h. The resulting mixture was concentrated under reduced pressure. The residue N-(4-chloro-3-(trifluoromethyl)phenyl)-3-fluoropyrrolidine-3-carboxamide was used for next step directly without further purification. LCMS: Method A, MS: ES+ 311.6.
  • Step c.
  • To a solution of N-(4-chloro-3-(trifluoromethyl)phenyl)-3-fluoropyrrolidine-3-carboxamide in EtOH (2 mL) was added cyanogen bromide (0.2 mmol) and NaHCO3 (0.6 mmol). The reaction mixture was stirred at rt for 16 h. The resulting mixture was concentrated under reduced pressure. The crude was purified by preparative reverse phase HPLC (A: 0.078% CH3COONH4 in water, B: MeCN) yielding (2.0 mg, 0.0059 mmol). LCMS: Method A, 2.50 min, MS: ES+ 336.0.
  • Compounds in Table 1 were synthesised using a procedure similar to that described for Example 1.
  • Figure US20180362460A1-20181220-C00012
  • TABLE 1
    LCMS LCMS RT MS
    Ex R Name Method (min) ES+
    2
    Figure US20180362460A1-20181220-C00013
         		1-cyano-3-fluoro-N-(4- phenylthiazol-2-yl)pyrrolidine-3- carboxamide B 2.58 317.4
    3
    Figure US20180362460A1-20181220-C00014
         		N-(benzo[d]thiazol-6-yl)-1-cyano- 3-fluoropyrrolidine-3-carboxamide B 2.30 291.3
    4
    Figure US20180362460A1-20181220-C00015
         		1-cyano-3-fluoro-N-(quinolin-3- yl)pyrrolidine-3-carboxamide B 2.20 285.3
    5
    Figure US20180362460A1-20181220-C00016
         		1-cyano-3-fluoro-N-(quinolin-6- yl)pyrrolidine-3-carboxamide B 1.59 285.3
    6
    Figure US20180362460A1-20181220-C00017
         		1-cyano-3-fluoro-N-(3-(2- methylthiazol-4- yl)phenyl)pyrrolidine-3- carboxamide B 2.39 331.4
    7
    Figure US20180362460A1-20181220-C00018
         		1-cyano-3-fluoro-N-(3- phenoxyphenyl)pyrrolidine-3- carboxamide B 2.43 326.3
    • Example 8 1-cyano-3-fluoro-N-(5-phenylthiazol-2-yl) pyrrolidine-3-carboxamide (Prepared According to General Scheme 1)
  • Figure US20180362460A1-20181220-C00019
  • Step a.
  • To a solution of 1-(tert-butoxycarbonyl)-3-fluoropyrrolidine-3-carboxylic acid (0.15 g, 0.64 mmol) in THF (10 ml) was added HBTU (0.48 g, 1.28 mmol) and DIPEA (0.25 g, 1.93 mmol) and stirred for 30 min at rt. The reaction mixture was treated with 5-phenylthiazol-2-amine (0.1 g, 0.58 mmol) and stirred for 18 h. The resulting reaction mixture was poured into NaHCO3 solution (50 ml) and extracted with EtOAc (2×15 ml). The combined organic phase was wash with brine (2×50 ml) and dried over Na2SO4, filtered and concentrated under reduced pressure yielding tert-butyl 3-fluoro-3-((5-phenylthiazol-2-yl)carbamoyl)pyrrolidine-1-carboxylate (0.25 g, 0.64 mmol), This material was used directly for the next step without further purification. LCMS: Method C, 2.38 min, MS: ES+ 336.2 (M-56).
  • Step b.
  • To a solution of tert-butyl 3-fluoro-3-((5-phenylthiazol-2-yl)carbamoyl)pyrrolidine-1-carboxylate (0.25 g, 0.64 mmol) in DCM (10 ml) was added TFA (1 ml) at 0° C. The reaction mixture was stirred for 1 h at rt. The resulting reaction mixture was concentrated under reduced pressure to obtained residue which was triturated in diethyl ether/n-pentane (20 ml) and evaporated to yielding 3-fluoro-N-(5-phenylthiazol-2-yl)pyrrolidine-3-carboxamide TFA salt (0.42 g, quantitative) LCMS: Method C, 1.59 min, MS: ES+ 292.18.
  • Step c.
  • To a solution 3-fluoro-N-(5-phenylthiazol-2-yl)pyrrolidine-3-carboxamide TFA salt (0.42 g, 1.03 mmol) in THF (10 ml) was added K2CO3 (0.58 g, 4.13 mmol) and cyanogen bromide (0.16 g, 1.55 mmol) at 0° C. The reaction mixture was stirred at rt for 30 min. The resulting mixture was poured into water (50 ml) and extracted with EtOAc (2×15 ml). The combined organic phase was washed with brine and dried over Na2SO4, filtered and concentrated under reduced pressure. The resulting residue was purified by column chromatography (35% EtOAc in hexane) yielding 1-cyano-3-fluoro-N-(5-phenylthiazol-2-yl)pyrrolidine-3-carboxamide (0.05 g, 0.16 mmol), LCMS: Method D, 3.95 min, MS: ES+ 317.2; 1H NMR (400 MHz, DMSO-d6) δ ppm 12.81 (S, 1H), 7.99 (s, 1H), 7.65 (d, J=7.2 Hz, 2H), 7.44 (t, J=8 Hz, 2H), 7.33 (t, J=7.2 Hz, 1H), 3.85-4.0 (m, 2H), 3.73-3.77 (m, 1H), 3.57-3.64 (m, 1H), 2.42-2.50 (m, 2H).
    • Example 9 (R)-1-cyano-3-fluoro-N-(5-phenylthiazol-2-yl) pyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00020
  • The title compound was isolated by chiral preparative HPLC of Example 8 to afford the desired enantiomer. LCMS: Method E, 2.54 min, MS: ES+ 317.0; 1H NMR (400 MHz, DMSO-d6) δ ppm 12.81 (s, 1H), 7.97 (s, 1H), 7.64 (d, J=8.4 Hz, 2H), 7.43 (t, J=7.6 Hz, 2H), 7.33 (t, J=7.6 Hz, 1H), 3.84-3.99 (m, 2H), 3.72-3.77 (m, 1H), 3.57-3.64 (m, 1H), 2.55-2.67 (m, 1H), 2.39-2.46 (m, 1H).
    • Example 10 1-cyano-3-fluoro-N-(5-phenylisoxazol-3-yl)pyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00021
  • The title compound was synthesised using a procedure similar to that described for Example 8. LCMS: Method D, 3.97 min, MS: ES+ 301.5; 1H NMR (400 MHz, DMSO-d6) δ ppm 11.57 (s, 1H), 7.90-7.92 (m, 2H), 7.52-7.57 (m, 3H), 7.36 (s, 1H), 3.94 (d, J=1.6 Hz, 1H), 3.87 (s, 1H), 3.72-3.78 (m, 1H), 3.57-3.61 (m, 1H), 2.54-2.57 (m, 1H), 2.41-2.45 (m, 1H).
    • Example 11 1-cyano-3-fluoro-N-(1-phenyl-1H-imidazol-4-yl)pyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00022
  • Step a. To a solution of 4-nitroimidazole (5 g, 44.2 mmol) in MeOH (40 ml) was added phenyl boronic acid (8.77 g, 71.66 mmol) at rt and treated with CuCl2 (0.71 g, 5.3 mmol) and NaOH (1.76 g, 44.2 mmol). The reaction mixture was stirred at 80° C. for 16 h whilst continuing the slow purging of O2 gas throughout the reaction time. The resulting reaction mixture was allowed to cool to rt and the purging of O2 gas was removed. The reaction mixture was then concentrated under reduced pressure. The obtained crude material was poured into water (500 ml) and extracted with EtOAc (3×150 ml). The combined organic phase was wash with NaHCO3 solution (200 ml) and dried over Na2SO4, filtered and concentrated under reduced pressure to yield 4-nitro-1-phenyl-1H-imidazole (1.5 g, 7.93 mmol), LCMS: Method C, 1.76 min, MS: ES+ 191.09.
  • Step b.
  • To a solution of 4-nitro-1-phenyl-1H-imidazole (0.17 g, 0.89 mmol) in THF (5 ml) was added 10% Pd/C (0.1 g), at rt. The reaction mixture was purged with H2 gas for 2 h at rt. The resulting reaction mixture was carefully filtered through celite hyflow and concentrated under reduced pressure to yield 1-phenyl-1H-imidazol-4-amine, LCMS: Method C, 2.86 min, MS: ES+ 159.93. This material was directly used for the next step without further purification.
  • Steps c-e.
  • The title compound was synthesised from the intermediate above using a procedure similar to that described for steps a-c of Example 8. LCMS: Method D, 3.29 min, MS: ES+ 300.3; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.89 (s, 1H), 8.19 (s, 1H), 7.79 (s, 1H), 7.65 (d, J=7.6 Hz, 2H), 7.52 (t, J=8.4 Hz, 2H), 7.37 (t, J=7.6 Hz, 1H), 3.94-3.90 (m, 1H), 3.71-3.87 (m, 2H), 3.55-3.62 (m, 1H), 2.38-2.50 (m, 2H).
    • Example 12 (S)-1-cyano-3-fluoro-N-(1-phenyl-1H-pyrazol-4-yl)pyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00023
  • The title compound was synthesised according to Example 8 and isolated by chiral preparative HPLC to afford the desired enantiomer. LCMS: Method D, 3.87 min, MS: ES+ 300.0; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.81 (s, 1H), 8.62 (s, 1H), 7.90 (s, 1H), 7.81 (d, J=7.6 Hz, 2H), 7.49 (t, J=8.4 Hz, 2H), 7.31 (t, J=7.6 Hz, 1H), 3.94-3.90 (m, 1H), 3.71-3.87 (m, 2H), 3.55-3.62 (m, 1H), 2.38-2.50 (m, 2H).
    • Example 13 (R)-1-cyano-3-fluoro-N-(1-phenyl-1H-pyrazol-4-yl)pyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00024
  • The title compound was synthesised according to Example 8 and isolated by chiral preparative HPLC to afford the desired enantiomer. LCMS: Method D, 3.87 min, MS: ES+ 300.0; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.81 (s, 1H), 8.62 (s, 1H), 7.90 (s, 1H), 7.80 (d, J=7.6 Hz, 2H), 7.50 (t, J=8.4 Hz, 2H), 7.31 (t, J=7.6 Hz, 1H), 3.94-3.90 (m, 1H), 3.71-3.87 (m, 2H), 3.55-3.62 (m, 1H), 2.38-2.50 (m, 2H).
    • Example 14 (R)-1-cyano-N-(1-(4-cyanophenyl)-1H-imidazol-4-yl)-3-fluoropyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00025
  • The title compound was synthesised using a procedure similar to that described for Example 11 and the single enantiomer separated by chiral prep. HPLC. LCMS: Method D, 3.32 min, MS: ES+ 325.5; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.98 (s, 1H), 8.40 (d, J=1.6 Hz, 1H), 8.00-8.02 (m, 2H), 7.91-7.94 (m, 3H), 3.91 (s, 1H), 3.83 (s, 1H), 3.71-3.74 (m, 1H), 3.58-3.62 (m, 1H), 2.57-2.59 (m, 1H), 2.42-2.45 (m, 1H).
    • Example 15 (R)—N-(1-benzyl-1H-pyrazol-4-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00026
  • The title compound was synthesised according to Example 8 and isolated by chiral preparative HPLC to afford the desired enantiomer. LCMS: Method F, 5.48 min, MS: ES+ 314.1; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.59 (s, 1H), 8.06 (s, 1H), 7.60 (s, 1H), 7.36-7.20 (m, 5H), 5.30 (s, 2H), 3.86-3.55 (m, 4H), 2.57-2.33 (m, 2H).
    • Example 16 N-(6-(1H-pyrazol-4-yl)benzo[d]thiazol-2-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00027
  • Step a.
  • To a stirred solution of 2-amino-6-bromobenzothiazole (0.3 g, 1.31 mmol) and pyrazole-4-boronic acid pinacol ester (0.63 g, 3.27 mmol) in DMF: water (10:3, 13 ml) was added CsF (0.63 g, 4.19 mmol) at rt in a microwave tube. The reaction mixture was degassed for 15 min at rt. Pd(PPh3)2Cl2 (0.14 g, 0.20 mmol) was added to the reaction mixture at rt. The reaction mixture was heated at 140° C. for 1 h in microwave. The resulting reaction mixture was allowed to cool at rt, poured into a solution of water: EtOAc (1:1, 60 ml) and filtered through celite bed. The organic phase was separated and the aqueous phase was re-extracted using EtOAc (30 ml) and 10% MeOH in DCM (2×30 ml). The combined organic phase was separated, dried over Na2SO4, filtered and concentrated under reduced pressure. The resulting residue was purified by flash chromatography (0-10% EtOAc in hexane, 5% MeOH in DCM) yielding 6-(1H-pyrazol-4-yl)benzo[d]thiazol-2-amine (0.22 g, 1.018 mmol). LCMS: Method C, 1.473 min, MS: ES+ 217.11; 1H NMR (400 MHz, DMSO-d6) δ ppm: 12.86 (s, 1H), 8.12 (s, 1H), 7.90 (s, 2H), 7.43-7.47 (m, 3H), 7.29 (d, J=8.4 Hz, 1H).
  • Steps b-d.
  • The title compound was synthesised from the intermediate above using a procedure similar to that described for steps a-c of Example 8. LCMS: Method D, 3.26 min, MS: ES+ 357.5; 1H NMR (400 MHz, DMSO-d6) δ ppm 12.96 (s, 2H), 8.25 (s 1H), 8.14 (br, s, 2H), 7.73 (s, 2H), 3.86-4.02 (m, 2H), 3.73-3.77 (m, 1H), 3.58-3.64 (m, 1H), 2.46-2.48 (m, 2H).
    • Example 17 1-cyano-3-fluoro-N-(6-phenylbenzo[d]thiazol-2-yl)pyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00028
  • The title compound was synthesised using a procedure similar to that described for Example 16 using phenylboronic acid. LCMS: Method F, 5.96 min, MS: ES+ 367.1; 1H NMR (400 MHz, DMSO-d6) δ ppm 12.98 (s, 1H), 8.37 (s, 1H), 7.86 (s, 1H), 7.74-7.80 (m, 3H), 7.49 (t, J=7.6 Hz, 2H), 7.38 (t, J=7.2 Hz, 1H), 3.91-4.03 (m, 2H), 3.74-3.79 (m, 1H), 3.59-3.65 (m, 1H), 2.59-2.62 (m, 2H).
    • Example 18 N-(5-(1H-indazol-4-yl) thiazol-2-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00029
  • Step a.
  • To a solution of 4-bromoindazole (1.0 g, 5.07 mmol) in DCM (20 ml) was added TEA (0.85 ml, 6.1 mmol) and DMAP (0.062 g, 0.50 mmol) at rt. Boc anhydride (1.28 ml, 5.58 mmol) was added drop wise to the reaction mixture at rt. The reaction mixture was stirred at rt for 2.5 h. The resulting reaction mixture was poured in to water (30 ml) and extracted with DCM (2×30 ml). The combined organic phase was dried over Na2SO4, filtered and concentrated under reduced pressure. The resulting residue was purified by flash chromatography (15-20% EtOAc in hexane) yielding tert-butyl 4-bromo-1H-indazole-1-carboxylate (1.5 g, 5.06 mmol). LCMS: Method C, 2.601 min, MS: ES+ 297.19; 1H NMR (400 MHz, DMSO-d6) δ ppm: 8.20 (s, 1H), 8.15 (d, J=8.0 Hz, 1H), 7.47 (dd, J=0.8 Hz, 7.6 Hz, 1H), 7.37-7.41 (m, 1H), 1.74 (s, 9H).
  • Step b.
  • To a stirred solution of tert-butyl 4-bromo-1H-indazole-1-carboxylate (0.3 g, 1.01 mmol) and tert-butyl (4-methoxybenzyl)(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazol-2-yl)carbamate (0.67 g, 1.515 mmol) in toluene:water (9:1, 10 ml) was added Na2CO3 (0.21 g, 2.02 mmol) at rt. The reaction mixture was degassed for 20 min at rt. Pd(dppf)Cl2 (0.074 g, 0.101 mmol) was added to the reaction mixture at rt. The reaction mixture was heated at 105° C. for 1 h. The resulting reaction mixture was allowed to cool at rt, poured into water (20 ml) and extracted with EtOAc (2×20 ml). The combined organic phase was separated, dried over Na2SO4, filtered and concentrated under reduced pressure. The resulting residue was purified by flash chromatography (7-20% EtOAc in hexane) yielding tert-butyl 4-(2-((tert-butoxycarbonyl)(4-methoxybenzyl)amino)thiazol-5-yl)-1H-indazole-1-carboxylate (0.44 g, 0.819 mmol). LCMS: Method C, 3.27 min, MS: ES+ 537.53.
  • Step c.
  • A solution of tert-butyl 4-(2-((tert-butoxycarbonyl)(4-methoxybenzyl)amino)thiazol-5-yl)-1H-indazole-1-carboxylate (0.42 g, 0.78 mmol) in TFA (10 ml) was heated to 85° C. for 3 h. The reaction mixture was allowed to cool at rt and excess of TFA was distilled under vacuum. The resulting reaction mixture was poured into a solution of water: EtOAc (1:1, 40 ml) and basified using solid NaHCO3. The organic layer was separated and aqueous layer was re-extracted with EtOAc (2×20 ml). The combined organic phase was separated, dried over Na2SO4, filtered and concentrated under reduced pressure. The resulting residue was purified by solvent trituration using DCM (5 ml) to yielding 5-(1H-indazol-4-yl)thiazol-2-amine (0.11 g, mmol). LCMS: Method C, 1.41 min, MS: ES+ 217.11; 1H NMR (400 MHz, DMSO-d6) δ ppm: 13.22 (s, 1H), 8.32 (s, 1H), 7.61 (s, 1H), 7.38 (d, J=8.4 Hz, 1H), 7.28-7.32 (m, 1H), 7.26 (s, 2H), 7.07 (d, J=7.2 Hz, 1H).
  • Steps d-f.
  • The title compound was synthesised from the intermediate above using a procedure similar to that described for steps a-c of Example 8. LCMS: Method E, 2.26 min, MS: ES+ 357.0; 1H NMR (400 MHz, DMSO-d6) δ ppm 13.37 (s, 1H), 12.88 (s, 1H), 8.41 (s, 1H), 8.16 (s, 1H), 7.55 (d, J=8.4 Hz, 1H), 7.41 (t, J=8.0 Hz, 1H), 7.34 (d, J=6.8 Hz, 1H), 3.96-4.02 (m, 1H), 3.91 (s, 1H), 3.74-3.79 (m, 1H), 3.59-3.66 (m, 1H), 2.56-2.62 (m, 2H).
    • Example 19 (R)—N-(5-(1H-indazol-7-yl)thiazol-2-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00030
  • Step a.
  • To a stirred solution of 1H-indazole-7-boronic acid (0.50 g, 3.09 mmol) and tert-butyl (5-bromothiazol-2-yl)(4-methoxybenzyl)carbamate (0.74 g, 1.85 mmol) in toluene:water (9:1, 20 ml) was added Na2CO3 (0.654 g, 6.17 mmol) at rt. The reaction mixture was degassed for 30 min at rt and then treated with Pd(dppf)Cl2 (0.22 g, 0.308 mmol). The reaction mixture was heated at 110° C. for 2 h. The resulting reaction mixture was allowed to cool to rt, poured into water (30 ml) and extracted with EtOAc (2×30 ml). The combined organic phase was separated, dried over Na2SO4, filtered and concentrated under reduced pressure. The resulting residue was purified by flash chromatography (22% EtOAc in hexane) yielding tert-butyl (5-(1H-indazol-7-yl)thiazol-2-yl)(4-methoxybenzyl)carbamate (0.575 g, 1.32 mmol). LCMS: Method C, 2.67 min, MS: ES+ 437.5; 1H NMR (400 MHz, DMSO-d6) δ ppm: 13.26 (s, 1H), 8.21-8.23 (m, 1H), 8.03 (s, 1H), 7.76 (d, J=8.0 Hz, 1H), 7.46 (d, J=7.2 Hz, 1H), 7.29 (d, J=8.4 Hz, 2H), 7.18 (t, J=7.6 Hz, 1H), 6.92 (d, J=8.8 Hz, 2H), 5.24 (s, 2H), 3.73 (s, 3H), 1.50 (s, 9H).
  • Step b.
  • A solution of tert-butyl (5-(1H-indazol-7-yl)thiazol-2-yl)(4-methoxybenzyl)carbamate (0.57 g, 1.30 mmol) in TFA (11.5 ml) was heated to 80° C. for 5 h. The resulting reaction mixture was allowed to cool to rt, poured into a solution of water: EtOAc (1:1, 60 ml) and basified using solid NaHCO3. The organic layer was separated and aqueous layer was re-extracted with EtOAc (30 ml). The combined organic phase was separated, dried over Na2SO4, filtered and concentrated under reduced pressure. The resulting residue was purified by solvent trituration using diethyl ether (2×10 ml) to 5-(1H-indazol-7-yl)thiazol-2-amine (0.274 g, 1.27 mmol). LCMS: Method C, 1.61 min, MS: ES+ 217.14; H NMR (400 MHz, DMSO-d6) δ ppm: 13.11 (s, 1H), 8.16 (s, 1H), 7.62-7.65 (m, 2H), 7.27 (s, 2H), 7.21 (d, J=7.2 Hz, 1H), 7.11 (t, J=7.2 Hz, 1H).
  • Steps c-e.
  • The title compound was synthesised from the intermediate above using a procedure similar to that described for steps a-c of Example 8. LCMS: Method D, 3.56 min, MS: ES+ 357.3; 1H NMR (400 MHz, DMSO-d6) δ ppm 13.87 (br, s, 1H), 13.25 (s, 1H), 8.22 (s, 1H), 8.09 (s, 1H), 7.75 (d, J=7.6 Hz, 1H), 7.46 (s, 1H), 7.16-7.20 (m, 1H), 3.98-4.01 (m, 1H), 3.85-3.93 (m, 1H), 3.73-3.77 (m, 1H), 3.57-3.64 (m, 1H), 2.56-2.59 (m, 2H).
    • Example 20 1-cyano-3-fluoro-N-(3-phenylisoxazol-5-yl)pyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00031
  • Step a.
  • To a solution of 3-phenylisoxazol-5-amine (0.137 g, 0.85 mmol) (CAS No: 4369-55-5, available from TCI India) and 1-(tert-butoxycarbonyl)-3-fluoropyrrolidine-3-carboxylic acid (0.2 g, 0.8536 mmol) in DCM (10 ml) was added pyridine (0.8 ml, 9.44 mmol) at 0° C. Phosphorous oxychloride (0.8 ml, 8.536 mmol) was added drop wise in to the reaction mixture at 0° C. The reaction mixture was stirred at rt for 30 min. The resulting reaction mixture was poured into 10% citric acid solution (100 ml) and extracted with DCM (3×50 ml). The combined organic phase was collected, dried over Na2SO4, filtered and concentrated under reduced pressure yielding tert-butyl 3-fluoro-3-((3-phenylisoxazol-5-yl)carbamoyl)pyrrolidine-1-carboxylate (0.33 g, quantitative). LCMS: Method C, 2.52 min, MS: ES− 374.6.
  • Steps b-c.
  • The title compound was synthesised from the intermediate above using a procedure similar to that described for steps b-c of Example 8. LCMS: Method E, 2.42 min, MS: ES+ 300.9; 1H NMR (400 MHz, DMSO-d6) δ ppm 12.28 (s, 1H), 7.86-7.89 (m, 2H), 7.51 (t, J=3.2 Hz, 3H), 6.88 (s, 1H), 3.84-3.97 (m, 2H), 3.73-3.78 (m, 1H), 3.58-3.65 (m, 1H), 2.33-2.47 (m, 2H).
    • Example 21 (R)-1-cyano-3-fluoro-N-(3-phenylisoxazol-5-yl)pyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00032
  • The title compound was isolated by chiral preparative HPLC of Example 20 to afford the desired enantiomer. LCMS: Method E, 2.36 min, MS: ES+ 300.9; 1H NMR (400 MHz, DMSO-d6) δ ppm 12.28 (s, 1H), 7.86-7.88 (m, 2H), 7.50-7.54 (m, 3H), 6.86 (s, 1H), 3.86-3.97 (m, 2H), 3.72-3.78 (m, 1H), 3.57-3.64 (m, 1H), 2.53-2.67 (m, 1H), 2.38-2.47 (m, 1H).
    • Example 22 N-(5-(3-carbamoylphenyl)thiazol-2-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00033
  • Step a.
  • To a solution of thiazol-2-amine (5 g, 49.9 mmol) in toluene (150 ml) was added 2,4-dimethoxybenzaldehyde (9.13 g, 54.9 mmol) and acetic acid (0.1 ml) at rt. The reaction mixture was heated at 130° C. for 20 h. The reaction mixture was concentrated under vacuum to remove toluene. The obtained residue was diluted with ethanol (75 ml) and DCM (75 ml). NaBH4 (3.02 g, 79.84 mmol) was added to the reaction mixture at 0° C. The reaction mixture was stirred at rt for 20 h. The resulting reaction mixture was poured into water (300 ml) and extracted with DCM (3×150 ml). The combined organic phase was wash with brine solution (150 ml), dried over Na2SO4, filtered and concentrated under reduced pressure. The resulting residue was purified by flash chromatography (30% EtOAc in hexane) yielding N-(2,4-dimethoxybenzyl)thiazol-2-amine (7 g, 28 mmol). MS: ES+ 251.32.
  • Step b.
  • To a solution of N-(2,4-dimethoxybenzyl)thiazol-2-amine (0.75 g, 2.99 mmol) in DMA (15 ml) were added 3-bromobenzamide (0.66 g, 3.29 mmol) and potassium acetate (0.74 g, 7.49 mmol) at rt. Degassed the reaction mixture for 15 min under N2. Tetrakis(triphenylphosphine)palladium(0) (0.173 g, 0.14 mmol) was added in to reaction mixture and heated at 160° C. for 4 h in microwave. The resulting reaction mixture was poured into water (200 ml) and extracted with ethyl acetate (3×100 ml). The combined organic phase was wash with brine solution (100 ml), dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was triturated with the diethyl ether (20 ml) and dried under vacuum to yielding 3-(2-((2,4-dimethoxybenzyl)amino)thiazol-5-yl)benzamide (0.66 g, 1.78 mmol). MS: ES+ 370.15.
  • Step c.
  • To a solution of 3-(2-((2,4-dimethoxybenzyl)amino)thiazol-5-yl)benzamide (0.66 g, 1.78 mmol) in DCM (20 ml) was added TFA (10 ml) at rt. The reaction mixture was stirred at rt for 4 h. The resulting reaction mixture was concentrated under reduced pressure. The obtained residue was diluted with ethyl acetate (100 ml) and wash with NaHCO3 solution (3×100 ml), brine (100 ml) and dried over Na2SO4, filtered and concentrated under reduced pressure to yielding 3-(2-aminothiazol-5-yl)benzamide (0.2 g, 0.91 mmol). MS: ES+ 220.19.
  • Steps b-d.
  • The title compound was synthesised from the intermediate above using a procedure similar to that described for steps a-c of Example 8. LCMS: Method E, 2.06 min, MS: ES+ 359.9; 1H NMR (400 MHz, DMSO-d6) δ ppm 12.84 (s, 1H), 8.11-8.13 (m, 2H), 8.05 (s, 1H), 7.80-7.82 (m, 2H), 7.49-7.53 (m, 2H), 3.89-4.00 (m, 2H), 3.73-3.77 (m, 1H), 3.58-3.64 (m, 1H), 2.45-2.50 (m, 2H).
    • Example 23 1-cyano-3-fluoro-N-(5-(3-(methylcarbamoyl)phenyl) thiazol-2-yl)pyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00034
  • Step a.
  • A suspension of 2-amino-5-bromothiazole hydrobromide (30.0 g, 116.35 mmol) and TEA (24.1 ml, 174.53 mmol) in THF (350 ml) was stirred at rt for 6 h. The resulting precipitate was removed by filtration and the filtrate was concentrated under reduced pressure yielding 2-amino-5-bromothiazole (17 g, 94.97 mmol). This material was immediately used for the next step without further purification.
  • Step b.
  • To a solution of 2-amino-5-bromothiazole (13 g, 72.62 mmol) and DMAP (0.44 g, 3.63 mmol) in THF (130 ml) was added (Boc)2O (15.83 g, 72.62 mmol) at rt. The reaction mixture was stirred at rt for 6 h. Excess THF was removed under reduced pressure and the resulting residue was purified by column chromatography (0-5% EtOAc in Hexane) yielding tert-butyl (5-bromothiazol-2-yl)carbamate (14.5 g, 52.16 mmol). LCMS: Method C, 2.28 min, MS: ES+ 279.08; 1H NMR (400 MHz, DMSO-d6) δ ppm 11.75 (s, 1H), 7.44 (s, 1H), 1.48 (s, 9H).
  • Step c.
  • A mixture of tert-butyl (5-bromothiazol-2-yl)carbamate (1.0 g, 3.60 mmol), triphenylphosphine (2.07 g, 7.91 mmol) and p-methoxybenzyl alcohol (0.99 g, 7.19 mmol) in THF (10 ml) was cooled at 0° C. DIAD (1.54 ml, 7.91 mmol) was added drop wise to the reaction mixture at 0° C. The reaction mixture was stirred at 0° C. for 10 min and then at rt for 2 h. The resulting reaction mixture was concentrated under reduced pressure and purified by flash chromatography (0-5% EtOAc in Hexane) yielding tert-butyl (5-bromothiazol-2-yl)(4-methoxybenzyl)carbamate (1.1 g, 2.76 mmol). LCMS: Method C, 3.02 min, MS: ES-56 343.1; 1H NMR (400 MHz, DMSO-d6) δ ppm 7.57 (s, 1H), 7.22 (d, J=8.4 Hz, 2H), 6.89 (d, J=8.4 Hz, 2H), 5.13 (s, 2H), 3.74 (s, 3H), 1.50 (s, 9H).
  • Step d.
  • A solution of tert-butyl (5-bromothiazol-2-yl)(4-methoxybenzyl)carbamate (1.05 g, 2.638 mmol) in dry THF (15 ml) was cooled at −78° C. 2.4M n-BuLi in Hexane (1.07 ml, 2.638 mmol) was added drop wise to the reaction mixture at −78° C. The reaction mixture was stirred at −78° C. for 20 min. 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (0.46 ml, 3.120 mmol) was added to the reaction mixture stirred for a further 30 min. The resulting reaction mixture was allowed to warm to 0° C. and quenched by addition of saturated ammonium chloride solution (100 ml). The resulting mixture was extracted with EtOAc (2×100 ml). The combined organic phase was dried over Na2SO4, filtered and concentrated under reduced pressure yielding tert-butyl (4-methoxybenzyl)(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazol-2-yl)carbamate (1.3 g, quantitative yield). This material was directly used for the next step without any purification.
  • Step e.
  • A solution of 3-bromobenzoic acid (2.0 g, 9.95 mmol) in THF (40 ml) were added HATU (5.60 g, 14.92 mmol) and DIPEA (3.40 ml, 19.90 mmol) at 0° C. The reaction mixture was stirred for 30 min at rt. Methylamine (2M in THF) (9.90 ml, 19.90 mmol) was added to the reaction mixture at rt and stirred for 18 h. The resulting reaction mixture was combined with one other batch on the same scale prepared by an identical method and poured into saturated NaHCO3 solution (100 ml). The resulting mixture was extracted with EtOAc (2×100 ml). The combined organic phase was dried over Na2SO4, filtered and concentrated under reduced pressure. The resulting residue was purified by flash chromatography (2-3% Methanol in DCM) yielding 3-bromo-N-methylbenzamide (4.13 g, 19.29 mmol). LCMS: Method C, 1.766 min, MS: ES+ 214.14.
  • Step f.
  • A suspension of 3-bromo-N-methylbenzamide (0.40 g, 1.87 mmol), tert-butyl (4-methoxybenzyl)(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazol-2-yl)carbamate (0.84 g, 1.87 mmol) and Na2CO3 (0.40 g, 3.74 mmol) in toluene: water (9:1) (15 ml) was degassed with nitrogen for 20 min at rt. Pd(dppf)Cl2 (0.14 g, 0.186 mmol) was added in to the reaction mixture at rt. The reaction mixture was heated at 105° C. for 2 h. The resulting reaction mixture was cooled to rt, poured into water (60 ml) and extracted with EtOAc (2×50 ml). The combined organic phase was dried over Na2SO4, filtered and concentrated under reduced pressure. The resulting residue was purified by flash chromatography (60% EtOAc in hexane) yielding tert-butyl (4-methoxybenzyl)(5-(3-(methylcarbamoyl)phenyl)thiazol-2-yl)carbamate (0.36 g, 0.79 mmol). LCMS: Method C, 2.66 min, MS: ES+ 454.55.
  • Step g.
  • A solution of tert-butyl (4-methoxybenzyl)(5-(3-(methylcarbamoyl)phenyl)thiazol-2-yl)carbamate (0.34 g, 0.750 mmol) in TFA (6.8 ml) was heated at 75° C. for 6 h. The resulting reaction mixture was concentrated under reduced pressure and saturated NaHCO3 solution (50 ml) was added in to resulting residue. The resulting mixture was extracted with EtOAc (3×50 ml). The combined organic phase was dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was triturated with n-hexane (2×5 ml) yielding 3-(2-aminothiazol-5-yl)-N-methylbenzamide (0.20 g, quantitative). This material was used for the next step without further purification. LCMS: Method C, 1.38 min, MS: ES+ 234.25.
  • Steps h-j.
  • The title compound was synthesised from the intermediate above using a procedure similar to that described for steps a-c of Example 8. LCMS: Method D, 3.27 min, MS: ES+ 374.5; 1H NMR (400 MHz, DMSO-d6) δ ppm 12.82 (br s, 1H), 8.60-8.59 (m, 1H), 8.06-8.05 (m, 2H), 7.82-7.79 (m, 2H), 7.52 (t, J=7.6, 1H), 3.89-4.00 (m, 2H), 3.73-3.78 (m, 1H), 3.58-3.64 (m, 1H), 2.81 (d, J=4.4, 3H), 2.45-2.52 (m, 2H).
    • Example 24 (R)-1-cyano-3-fluoro-N-(5-(3-(methylcarbamoyl)phenyl)thiazol-2-yl)pyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00035
  • The title compound was isolated by chiral preparative HPLC of Example 23 to afford the desired enantiomer. LCMS: Method D, 3.27 min, MS: ES+ 374.5; 1H NMR (400 MHz, DMSO-d6) δ ppm 12.84 (br s, 1H), 8.59-8.60 (m, 1H), 8.06-8.05 (m, 2H), 7.80-7.70 (m, 2H), 7.52 (t, J=7.6, 1H), 3.89-4.00 (m, 2H), 3.73-3.78 (m, 1H), 3.58-3.64 (m, 1H), 2.81 (d, J=4.4, 3H), 2.45-2.52 (m, 2H).
    • Example 25 N-(5-(3-(1H-imidazol-1-yl)phenyl)thiazol-2-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00036
  • Step a.
  • A suspension of 1,3-dibromobenzene (2.0 g, 8.48 mmol) in DMSO (7.8 ml) was added 1H-imidazole (0.58 g, 8.48 mmol) and K2CO3 (2.34 g, 16.96 mmol). The reaction mixture was degassed with nitrogen for 10 min at rt. CuI (0.002 g) was added at rt and the reaction mixture was heated at 160° C. for 1 h in microwave. The resulting reaction mixture was poured into water (20 ml) and extracted with EtOAc (5×10 ml). The combined organic phase was collected, dried over Na2SO4, filtered and concentrated under reduced pressure yielding 1-(3-bromophenyl)-1H-imidazole (1.0 g, 4.48 mmol). LCMS: Method C, 1.53 min, MS: ES+ 223.1.
  • Step b.
  • A solution of 1-(3-bromophenyl)-1H-imidazole (0.25 g, 1.12 mmol) and tert-butyl (4-methoxybenzyl)(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazol-2-yl)carbamate (1.00 g, 2.24 mmol) in toluene was degassed with nitrogen for 15 min at rt. NH4OH (0.08 g, 2.24 mmol) and Pd(dppf)Cl2 (0.08 g, 0.11 mmol) were added to the reaction mixture at rt. The resulting reaction mixture was stirred at rt for 2 h and then heated at 80° C. for 2 h. The resulting reaction mixture was cooled to rt, poured into water (100 ml) and extracted with EtOAc (2×100 ml). The combined organic phase was washed with brine solution (75 ml), dried over Na2SO4, filtered and concentrated under reduced pressure. The resulting residue was purified by flash chromatography (12.6% EtOAc in hexane) yielding tert-butyl (5-(3-(1H-imidazol-1-yl)phenyl)thiazol-2-yl)(4-methoxybenzyl)carbamate (0.40 g, 0.86 mmol). LCMS: Method C, 2.37 min, MS: ES+ 463.3; 1H NMR (400 MHz, DMSO-d6) δ ppm 8.38 (s, 1H), 8.05 (s, 1H), 7.86-7.90 (m, 2H), 7.53-7.60 (m, 3H), 7.27 (d, J=8.8 Hz, 2H), 7.13 (s, 1H), 6.90 (d, J=8.8 Hz, 2H), 5.21 (s, 2H), 3.72 (s, 3H), 1.50 (s, 9H).
  • Step c.
  • A solution of tert-butyl (5-(3-(1H-imidazol-1-yl)phenyl)thiazol-2-yl)(4-methoxybenzyl)carbamate (0.40 g, 0.86 mmol) in TFA (8 ml) was heated at 80° C. for 3 h. The resulting reaction mixture was concentrated under reduced pressure and saturated NaHCO3 solution (100 ml) was added in to resulting residue. The resulting mixture was extracted with EtOAc (2×100 ml). The combined organic phase was washed with brine solution (75 ml), dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was triturated with diethyl ether (20 ml) yielding 5-(3-(1H-imidazol-1-yl)phenyl)thiazol-2-amine (0.15 g, 0.62 mmol). LCMS: Method F, 5, 2.56 min, MS: ES+ 242.89; 1H NMR (400 MHz, DMSO-d6) δ ppm 8.33 (s, 1H), 7.82 (s, 1H), 7.72 (s, 1H), 7.61 (s, 1H), 7.41-7.49 (m, 2H), 7.24-7.34 (m, 3H), 7.11 (s, 1H).
  • Steps d-f.
  • The title compound was synthesised from the intermediate above using a procedure similar to that described for steps a-c of Example 8. LCMS: Method E, 2.37 min, MS: ES+ 382.9, 1H NMR (400 MHz, DMSO-d6) δ ppm 12.90 (br s, 1H), 8.40 (s, 1H), 8.18 (s, 1H), 7.97 (d, J=1.6 Hz, 1H), 7.89 (s, 1H), 7.54-7.63 (m, 3H), 7.14 (s, 1H), 3.89-4.00 (m, 2H), 3.73-3.78 (m, 1H), 3.58-3.64 (m, 1H), 2.43-2.50 (m, 2H).
    • Example 26 N-(3-(3-(1H-imidazol-1-yl)phenyl)isoxazol-5-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00037
  • Step a.
  • To a solution of acetonitrile (0.78 ml, 14.851 mmol) in dry THF (20 ml) was added n-BuLi (1.6 M in n-Hexane) (12.38 ml, 19.80 mmol) at −78° C. After 90 min a solution of methyl 3-(1H-imidazol-1-yl)benzoate (CAS Number 335255-85-1) (1.0 g, 4.95 mmol) in dry THF (5 ml) was added slowly to the reaction mixture at −78° C. and the reaction mixture was stirred at −78° C. for 2 h. The resulting reaction mixture was quenched by addition of NH4Cl solution (7-8 ml) and reaction mixture was concentrated under reduced pressure. The resulting residue was purified by flash chromatography (2-4% MeOH in DCM) yielding 3-(3-(1H-imidazol-1-yl) phenyl)-3-oxopropanenitrile (0.8 g, 3.79 mmol). 1H NMR (400 MHz, DMSO-d6) δ ppm 8.44 (s, 1H), 8.16 (t, J=1.6 Hz, 1H), 8.00-8.03 (m, 1H), 7.89-7.92 (m, 2H), 7.72 (t, J=8 Hz, 1H), 7.19 (s, 1H), 4.85 (s, 2H).
  • Step b.
  • To a solution of 3-(3-(1H-imidazol-1-yl)phenyl)-3-oxopropanenitrile (0.8 g, 3.79 mmol) in ethanol (25 ml) were added hydroxylamine hydrochloride (0.52 g, 7.58 mmol) and NaOAc (0.62 g, 7.58 mmol) at rt. The resulting reaction mixture was heated at reflux for 4 h. The resulting reaction mixture was cooled to rt, poured into water (50 ml) and extracted with EtOAc (3×20 ml). The combined organic phase was washed with brine solution (2×30 ml), dried over Na2SO4, filtered and concentrated under reduced pressure yielding 3-(3-(1H-imidazol-1-yl)phenyl)isoxazol-5-amine (0.8 g, 3.538 mmol). LCMS: Method C, 1.34 min, MS: ES+ 227.35; 1H NMR (400 MHz, DMSO-d6) δ ppm 8.36 (s, 1H), 7.94 (t, J=1.6 Hz, 1H), 7.86 (t, J=1.2 Hz, 1H), 7.71-7.74 (m, 2H), 7.58 (t, J=8 Hz, 1H), 7.13 (s, 1H), 6.87 (s, 2H), 5.58 (s, 1H).
  • Steps c-e.
  • The title compound was synthesised from the intermediate above using a procedure similar to that described for steps a-c of Example 8. LCMS: Method E, 2.18 min, MS: ES+ 367.0; 1H NMR (400 MHz, DMSO-d6) δ ppm 12.33 (s, 1H), 8.43 (s, 1H), 8.15 (t, J=2 Hz 1H), 7.93 (s, 1H), 7.88 (d, J=7.6 Hz, 1H), 7.80-7.83 (m, 1H), 7.65 (t, J=7.6 Hz, 1H), 7.16 (s, 1H), 7.14 (s, 1H), 3.95 (s, 1H), 3.88 (s, 1H), 3.74-3.79 (m, 1H), 3.59-3.65 (m, 1H), 2.44-2.54 (m, 2H).
    • Example 27 (R)—N-(3-(3-(1H-imidazol-1-yl)phenyl)isoxazol-5-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00038
  • The title compound was isolated by chiral preparative HPLC of Example 26 to afford the desired enantiomer. LCMS: Method E, 2.18 min, MS: ES+ 367.0; 1H NMR (400 MHz, DMSO-d6) δ ppm 12.33 (s, 1H), 8.43 (s, 1H), 8.15 (t, J=2 Hz 1H), 7.93 (s, 1H), 7.88 (d, J=7.6 Hz, 1H), 7.80-7.83 (m, 1H), 7.65 (t, J=7.6 Hz, 1H), 7.16 (s, 1H), 7.14 (s, 1H), 3.95 (s, 1H), 3.88 (s, 1H), 3.74-3.79 (m, 1H), 3.59-3.65 (m, 1H), 2.44-2.54 (m, 2H).
    • Example 28 N-(6-(1H-pyrazol-5-yl)imidazo[1,2-a]pyridin-2-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00039
  • Step a.
  • 6-bromoimidazo[1,2-a]pyridin-2-amine and tert-butyl 3-fluoro-3-formylpyrrolidine-1-carboxylate were used in a procedure similar to that described for step a of Example 8 to afford tert-butyl 3-((6-bromoimidazo[1,2-a]pyridin-2-yl)carbamoyl)-3-fluoropyrrolidine-1-carboxylate.
  • Step b.
  • tert-butyl 3-((6-bromoimidazo[1,2-a]pyridin-2-yl)carbamoyl)-3-fluoropyrrolidine-1-carboxylate and (1H-pyrazol-5-yl)boronic acid were used in a procedure similar to Example 21 step a to afford tert-butyl 3-((6-(1H-pyrazol-5-yl)imidazo[1,2-a]pyridin-2-yl)carbamoyl)-3-fluoropyrrolidine-1-carboxylate.
  • Steps c-d.
  • The title compound was synthesised from the intermediate above using a procedure similar to that described for steps b-c of Example 8. LCMS: Method D, 2.86 min, MS: ES+ 340.5; 1H NMR (400 MHz, DMSO-d6) δ ppm 12.98 (s, 1H), 11.13 (s, 1H), 9.05 (s, 1H), 8.21 (s, 1H), 7.84 (s, 1H), 7.75 (d, J=9.2 Hz, 1H), 7.50 (d, J=9.2 Hz, 1H), 6.72 (s, 1H), 3.87-4.05 (m, 1H), 3.81 (s, 1H), 3.72-3.78 (m, 1H), 3.57-3.63 (m, 1H), 2.57-2.61 (m, 1H), 2.38-2.45 (m, 1H).
    • Example 29 1-cyano-3-fluoro-N-(6-(3-(methylcarbamoyl)phenyl)benzo[d]thiazol-2-yl)pyrrolidine-3-carboxamide
  • Figure US20180362460A1-20181220-C00040
  • The title compound was synthesised using a procedure similar to that described for Example 28 using 6-bromobenzo[d]thiazol-2-amine and tert-butyl 3-fluoro-3-formylpyrrolidine-1-carboxylate. LCMS: Method D, 3.64 min, MS: ES+ 424.6; 1H NMR (400 MHz, DMSO-d6) δ ppm 12.95 (br, s, 1H), 8.55-8.61 (m, 1H), 8.38 (s, 1H), 8.19 (s, 1H), 7.82-7.89 (m, 4H), 7.57 (t, J=9.6, 1H), 4.00-4.03 (m, 1H), 3.85-3.95 (m, 2H), 3.74-3.78 (m, 1H), 3.58-3.65 (m, 1H), 3.42-3.46 (m, 1H), 2.83 (d, J=4.4 Hz, 3H).
    • Biological Activity of Compounds of the Invention Abbreviations
  • TAMRA carboxytetramethylrhodamine
  • PCR polymerase chain reaction
  • PBS phosphate buffered saline
  • EDTA ethylenediaminetetraacetic acid
  • Tris 2-amino-2-(hydroxymethyl)-1,3-propanediol
  • NP-40 Nonidet P-40, octylphenoxypolyethoxyethanol
  • BSA bovine serum albumin
  • DMSO dimethyl sulfoxide
    • In Vitro Cezanne 1 Inhibition Assay Expression and Purification of Cezanne 1
  • The Cezanne 1 construct was PCR amplified and cloned into a pFLAG-CMV-6c vector (Sigma-Aldrich) with an N-terminal FLAG tag. HEK293T cells were transfected with FLAG-Cezanne 1 using TransIT-LT1 transfection reagent (Mirus) according to the manufacturer's instructions. Cells were harvested 48 hours after transfection. Cells were washed once with PBS and scraped in lysis buffer (50 mM Tris, pH 7.5, 150 mM NaCl, 3 mM EDTA, 0.5% NP40, 10% glycerol, 5 mM beta-mercaptoethanol, protease inhibitors (complete mini, Roche) and phosphatase inhibitors (PhosSTOP mini, Roche). Lysates were incubated for 30 min on ice and centrifuged at 4000 rpm for 10 min at 4° C. Soluble supernatant was added to FLAG affinity resin (EZview Red ANTI-FLAG M2 affinity gel, Sigma-Aldrich) equilibrated in low salt buffer (20 mM Tris, pH 7.5, 150 mM NaCl, 0.5 mM EDTA, 5 mM beta-mercaptoethanol) and incubated at 4° C. for 3 hours rotating. The resin was spun at 2000 rpm for 2 min and the supernatant was removed. The resin was washed two times with low salt buffer and one time with high salt buffer (20 mM Tris, pH 7.5, 500 mM NaCl, 0.5 mM EDTA, 5 mM beta-mercaptoethanol, protease inhibitors (complete mini, Roche) and phosphatase inhibitors (PhosSTOP mini, Roche). To elute the bound Cezanne 1, elution buffer (10 mM Tris, pH 7.5, 150 mM NaCl, 0.5 mM EDTA, 10% glycerol, 0.5% NP40, 5 mM beta-mercaptoethanol, 0.15 mg/ml 3× FLAG peptide (Sigma-Aldrich)) was added to the resin and incubated at 4° C. for 2.5 hours while rotating. The resin was centrifuged at 4000 rpm for 30 seconds, and the supernatant containing purified FLAG-Cezanne 1 was removed and stored at −80° C.
    • Cezanne 1 Biochemical Kinetic Assay
  • Reactions were performed in duplicate in black 384 well plates (small volume, Greiner 784076) in a final reaction volume of 21 μl. Cezanne 1 was diluted in reaction buffer (40 mM Tris, pH 7.5, 0.005% Tween 20, 0.5 mg/ml BSA, 5 mM—beta-mercaptoethanol) to the equivalent of 0, 0.001, 0.050, 0.01 and 0.05 μl/well. Buffer was optimised for optimal temperature, pH, reducing agent, salts, time of incubation, and detergent. Reactions were initiated by the addition of 50 nM of TAMRA labelled peptide linked to ubiquitin via an iso-peptide bond as fluorescence polarisation substrate. Reactions were incubated at room temperature and read every 2 min for 120 min. Readings were performed on a Pherastar Plus (BMG Labtech). λ Excitation 540 nm; λ Emission 590 nm.
    • Cezanne 1 Biochemical IC50 Assay
  • Dilution plates were prepared at 21 times the final concentration (2100 μM for a final concentration of 100 μM) in 50% DMSO in a 96-well polypropylene V-bottom plate (Greiner #651201). A typical 8-point dilution series to be 100, 30, 10, 3, 1, 0.3, 0.1, 0.03 M final. Reactions were performed in duplicate in black 384 well plates (small volume, Greiner 784076) in a final reaction volume of 21 μl. Either 1 μl of 50% DMSO or diluted compound was added to the plate. Cezanne 1 was diluted in reaction buffer (40 mM Tris, pH 7.5, 0.005% Tween 20, 0.5 mg/ml BSA, 5 mM—beta-mercaptoethanol) to the equivalent of 0.005 μl/well and 10 μl of diluted Cezanne 1 was added to the compound. Enzyme and compound were incubated for 30 min at room temp. Reactions were initiated by the addition of 50 nM of TAMRA labelled peptide linked to ubiquitin via an iso-peptide bond as fluorescence polarisation substrate. Reactions were read immediately after addition of substrate and following a 2 hr incubation at room temperature. Readings were performed on a Pherastar Plus (BMG Labtech). λ Excitation 540 nm; λ Emission 590 nm.
  • Activity of Exemplary Compounds in Cezanne 1 biochemical IC50 assay Ranges:
  • A<0.1 μM;
  • 0.1<B<1 μM;
  • 1<C<10 μM
  • Example IC50 range
    1 C
    2 C
    3 B
    4 C
    5 C
    6 C
    7 C
    8 B
    9 B
    10 B
    11 C
    12 C
    13 A
    14 C
    15 C
    16 C
    17 C
    18 B
    19 B
    20 B
    21 B
    22 B
    23 B
    24 B
    25 B
    26 B
    27 B
    28 B
    29 C

Claims (16)

1. A compound with the formula (I):
Figure US20180362460A1-20181220-C00041
or a pharmaceutically acceptable salt thereof, wherein:
R1a, R1b, R1c and R1d each independently represent hydrogen or an optionally substituted C1-C6 alkyl, or R1a is linked to R1b to form an optionally substituted cycloalkyl ring, or R1d is linked to R1c or R1e to form an optionally substituted cycloalkyl ring;
R1e and R1f each independently represent hydrogen, fluorine, cyano, hydroxyl, amino, optionally substituted C1-C6 alkyl, optionally substituted C1-C6 alkoxy or an optionally substituted 5 or 6 membered heteroaryl or aryl ring, or R1e and R1f together form an optionally substituted cycloalkyl ring, or R1e is linked to R1d to form an optionally substituted cycloalkyl ring;
A is an optionally substituted 5 to 10 membered heteroaryl or aryl ring.
2. The compound according to claim 1, wherein ring A is substituted with one or more of -Q1(R2)n, wherein each occurrence of -Q1(R2)n is the same or different, wherein:
n is 0 or 1;
Q1 represents halogen, cyano, oxo, nitro, —OR3, —SR3, —NR3R4, —CONR3R4, —NR3COR4, —NR3CONR4R5, —COR3, —C(O)OR3, —SO2R3, —SO2NR3R4, —NR3SO2R4, —NR3SO2NR4R5, —NR3C(O)OR4, optionally substituted —C1-C6 alkyl, optionally substituted —C1-C6 alkoxy, optionally substituted —C2-C6 alkenyl, a covalent bond, an oxygen atom, a sulphur atom, —SO—, —SO2-, —CO—, —C(O)O—, —CONR3—, —NR3-, —NR3CO—, —NR3CONR4—, —SO2NR3—, —NR4SO2—, —NR3SO2NR4—, —NR3C(O)O—, —NR3C(O)OR4—, optionally substituted C1-C6 alkylene, or optionally substituted —C2-C6 alkenylene;
R2 is an optionally substituted 3 to 10 membered ring;
R3, R4 and R5 each independently represent hydrogen, optionally substituted C1-C6 alkyl or optionally substituted C1-C6 alkylene.
3. The compound according to claim 2, wherein R2 represents a 3 to 10 membered ring which is unsubstituted or substituted with one or more substituents selected from halogen, cyano, oxo, nitro, —OR6, —SR6, —NR6R7, —CONR6R7, —NR6COR7, —NR6CONR7R8, —COR6, —C(O)OR6, —SO2R6, —SO2NR6R7, —NR6SO2R7, —NR6SO2NR7R8, —NR6C(O)OR7, optionally substituted —C1-C6 alkyl, optionally substituted —C1-C6 alkoxy, optionally substituted —C2-C6 alkenyl, optionally substituted C2-C6 alkynyl, -Q2-R6, -Q2-NR6CONR7R8, -Q2-NR6R7, -Q2_COR6, -Q2-NR6COR7, -Q2-NR6C(O)OR7, -Q2-SO2R6, Q2-CONR6R7, -Q2-CO2R6, -Q2-SO2NR6R7, -Q2-NR6SO2R7 and -Q2-NR6SO2NR7R8;
Q2 represents a covalent bond, an oxygen atom, a sulphur atom, —SO—, —SO2—, —CO—, or a C1-C6 alkylene, or optionally substituted C2-C6 alkenylene; and
R6, R7, R8 each independently represent hydrogen, optionally substituted C1-C6 alkyl, optionally substituted heterocyclyl, optionally substituted heteroaryl, optionally substituted aryl, or an optionally substituted cycloalkyl.
4. The compound according to claim 1, wherein ring A is a 5 or 6 membered optionally substituted heteroaryl or aryl ring.
5. The compound according to claim 1, wherein ring A is a 9 or 10 membered optionally substituted heteroaryl or aryl ring.
6. The compound according to claim 1, wherein ring A is a nitrogen containing heteroaryl ring.
7. The compound according to claim 1, wherein A is a 5 to 10 membered heteroaryl or aryl ring selected from thiazolyl, imidazolyl, isoxazolyl, pyrazolyl, phenyl, benzothiazolyl, imidazopyridinyl and quinolinyl.
8. The compound according to claim 1, wherein R1a, R1b, R1c, R1d, R1e and R1f are each hydrogen.
9. The compound according to claim 1, wherein R2 represents an optionally substituted 3 to 10 membered ring selected from pyrazolyl, thiazolyl, phenyl and indazolyl.
10. The compound according to claim 1, wherein C1-C6 alkyl, C1-C6 alkoxy, C2-C6 alkenyl, C2-C6 alkynyl, C1-C6 alkylene, C1-C6 alkyleneoxy, C2-C6 alkenylene are each independently optionally substituted with one or more substituents selected from halogen, hydroxyl, thiol, cyano, amino, nitro and SF5.
11. The compound according to claim 1, having the formula (II):
Figure US20180362460A1-20181220-C00042
or a pharmaceutically acceptable salt thereof, wherein:
R1a, R1b, R1c and R1d each independently represent hydrogen or an optionally substituted C1-C6 alkyl, or R1a is linked to R1b to form an optionally substituted cycloalkyl ring, or R1d is linked to R1c or R1e to form an optionally substituted cycloalkyl ring;
R1e and R1f each independently represent hydrogen, fluorine, cyano, hydroxyl, amino, optionally substituted C1-C6 alkyl, optionally substituted C1-C6 alkoxy or an optionally substituted 5 or 6 membered ring, or R1e and R1f together form an optionally substituted cycloalkyl ring, or R1e is linked to R1d to form an optionally substituted cycloalkyl ring;
A is an optionally substituted 5 to 10 membered heteroaryl or aryl ring.
12. The compound according to claim 1, selected from the group consisting of:
N-(4-chloro-3-(trifluoromethyl)phenyl)-1-cyano-3-fluoropyrrolidine-3-carboxamide;
1-cyano-3-fluoro-N-(4-phenylthiazol-2-yl)pyrrolidine-3-carboxamide;
N-(benzo[d]thiazol-6-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide;
1-cyano-3-fluoro-N-(quinolin-3-yl)pyrrolidine-3-carboxamide;
1-cyano-3-fluoro-N-(quinolin-6-yl)pyrrolidine-3-carboxamide;
1-cyano-3-fluoro-N-(3-(2-methylthiazol-4-yl)phenyl)pyrrolidine-3-carboxamide;
1-cyano-3-fluoro-N-(3-phenoxyphenyl)pyrrolidine-3-carboxamide;
1-cyano-3-fluoro-N-(5-phenylthiazol-2-yl)pyrrolidine-3-carboxamide;
(R)-1-cyano-3-fluoro-N-(5-phenylthiazol-2-yl)pyrrolidine-3-carboxamide;
1-cyano-3-fluoro-N-(5-phenylisoxazol-3-yl)pyrrolidine-3-carboxamide;
1-cyano-3-fluoro-N-(1-phenyl-1H-imidazol-4-yl)pyrrolidine-3-carboxamide;
(S)-1-cyano-3-fluoro-N-(1-phenyl-1H-pyrazol-4-yl)pyrrolidine-3-carboxamide;
(R)-1-cyano-3-fluoro-N-(1-phenyl-1H-pyrazol-4-yl)pyrrolidine-3-carboxamide;
(R)-1-cyano-N-(1-(4-cyanophenyl)-1H-imidazol-4-yl)-3-fluoropyrrolidine-3-carboxamide;
(R)—N-(1-benzyl-1H-pyrazol-4-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide;
N-(6-(1H-pyrazol-4-yl)benzo[d]thiazol-2-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide;
1-cyano-3-fluoro-N-(6-phenylbenzo[d]thiazol-2-yl)pyrrolidine-3-carboxamide;
N-(5-(1H-indazol-4-yl)thiazol-2-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide;
(R)—N-(5-(1H-indazol-7-yl)thiazol-2-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide;
1-cyano-3-fluoro-N-(3-phenylisoxazol-5-yl)pyrrolidine-3-carboxamide;
(R)-1-cyano-3-fluoro-N-(3-phenylisoxazol-5-yl)pyrrolidine-3-carboxamide;
N-(5-(3-carbamoylphenyl)thiazol-2-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide;
1-cyano-3-fluoro-N-(5-(3-(methylcarbamoyl)phenyl)thiazol-2-yl)pyrrolidine-3-carboxamide;
(R)-1-cyano-3-fluoro-N-(5-(3-(methylcarbamoyl)phenyl)thiazol-2-yl)pyrrolidine-3-carboxamide;
N-(5-(3-(1H-imidazol-1-yl)phenyl)thiazol-2-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide;
N-(3-(3-(1H-imidazol-1-yl)phenyl)isoxazol-5-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide;
(R)—N-(3-(3-(1H-imidazol-1-yl)phenyl)isoxazol-5-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide;
N-(6-(1H-pyrazol-5-yl)imidazo[1,2-a]pyridin-2-yl)-1-cyano-3-fluoropyrrolidine-3-carboxamide; and
1-cyano-3-fluoro-N-(6-(3-(methylcarbamoyl)phenyl)benzo[d]thiazol-2-yl)pyrrolidine-3-carboxamide,
or a pharmaceutically acceptable salt thereof.
13. A process for the preparation of a compound of formula (I) or a pharmaceutically acceptable salt thereof as defined according to claim 1 which comprises reacting an amine of formula (IV) with cyanogen bromide:
Figure US20180362460A1-20181220-C00043
wherein R1a, R1b, R1c, R1d, R1e, R1f and A are as defined in claim 1.
14. A method for treating cancer, comprising the step of administering a compound according to claim 1, or a pharmaceutically acceptable salt thereof, to a patient in need thereof.
15. A method for treating a condition involving mitochondrial dysfunction, comprising the step of administering a compound according to claim 1, or a pharmaceutically acceptable salt thereof, to a patient in need thereof.
16. A pharmaceutical composition, comprising a compound according to claim 1, or a pharmaceutically acceptable salt thereof together, with one or more pharmaceutically acceptable excipients.
US16/060,299 2015-12-23 2016-12-21 Cyanopyrrolidine derivatives as inhibitors for DUBs Active US10590075B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB1522768.9 2015-12-23
GBGB1522768.9A GB201522768D0 (en) 2015-12-23 2015-12-23 Novel compounds
PCT/GB2016/054022 WO2017109488A1 (en) 2015-12-23 2016-12-21 Cyanopyrrolidine dervivatives as inhibitors for dubs

Publications (2)

Publication Number Publication Date
US20180362460A1 true US20180362460A1 (en) 2018-12-20
US10590075B2 US10590075B2 (en) 2020-03-17

Family

ID=55311537

Family Applications (1)

Application Number Title Priority Date Filing Date
US16/060,299 Active US10590075B2 (en) 2015-12-23 2016-12-21 Cyanopyrrolidine derivatives as inhibitors for DUBs

Country Status (6)

Country Link
US (1) US10590075B2 (en)
EP (1) EP3394049B1 (en)
JP (1) JP6810148B2 (en)
CN (1) CN108290872B (en)
GB (1) GB201522768D0 (en)
WO (1) WO2017109488A1 (en)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MD3277677T2 (en) 2015-03-30 2021-07-31 Mission Therapeutics Ltd 1-cyano-pyrrolidine compounds as usp30 inhibitors
EP3322702B1 (en) 2015-07-14 2019-11-20 Mission Therapeutics Limited Cyanopyrrolidines as dub inhibitors for the treatment of cancer
GB201521109D0 (en) 2015-11-30 2016-01-13 Mission Therapeutics Ltd Novel compounds
GB201522267D0 (en) 2015-12-17 2016-02-03 Mission Therapeutics Ltd Novel compounds
GB201522768D0 (en) 2015-12-23 2016-02-03 Mission Therapeutics Ltd Novel compounds
GB201602854D0 (en) 2016-02-18 2016-04-06 Mission Therapeutics Ltd Novel compounds
GB201603779D0 (en) 2016-03-04 2016-04-20 Mission Therapeutics Ltd Novel compounds
GB201604647D0 (en) 2016-03-18 2016-05-04 Mission Therapeutics Ltd Novel compounds
GB201604638D0 (en) 2016-03-18 2016-05-04 Mission Therapeutics Ltd Novel compounds
EP3433246B1 (en) 2016-03-24 2022-05-04 Mission Therapeutics Limited 1-cyano-pyrrolidine derivatives as dbu inhibitors
ES2850349T3 (en) 2016-09-27 2021-08-27 Mission Therapeutics Ltd Cyanopyrrolidine derivatives with activity as USP30 inhibitors
GB201616511D0 (en) 2016-09-29 2016-11-16 Mission Therapeutics Limited Novel compounds
GB201616627D0 (en) 2016-09-30 2016-11-16 Mission Therapeutics Limited Novel compounds
TWI771327B (en) 2016-10-05 2022-07-21 英商使命醫療公司 Novel compounds
GB201708652D0 (en) 2017-05-31 2017-07-12 Mission Therapeutics Ltd Novel compounds and uses
EP3642196B1 (en) 2017-06-20 2022-08-17 Mission Therapeutics Limited Substituted cyanopyrrolidines with activity as dub inhibitors
AU2018346597B2 (en) 2017-10-06 2023-07-13 Forma Therapeutics, Inc. Inhibiting Ubiquitin Specific Peptidase 30
WO2020036940A1 (en) 2018-08-14 2020-02-20 Amgen Inc. N-cyano-7-azanorbornane derivatives and uses thereof
BR112021003620A2 (en) 2018-10-05 2021-05-18 Forma Therapeutics, Inc. Fused pyrrolines that act as specific protease inhibitors for ubiquitin 30 (usp30)
GB201905371D0 (en) 2019-04-16 2019-05-29 Mission Therapeutics Ltd Novel compounds
GB201905375D0 (en) 2019-04-16 2019-05-29 Mission Therapeutics Ltd Novel compounds
GB201912674D0 (en) 2019-09-04 2019-10-16 Mission Therapeutics Ltd Novel compounds
CA3171349A1 (en) 2020-04-08 2021-10-14 Mission Therapeutics Limited N-cyanopyrrolidines with activity as usp30 inhibitors
US20230219939A1 (en) 2020-05-28 2023-07-13 Mission Therapeutics Limited N-(1-cyano-pyrrolidin-3-yl)-5-(3-(trifluoromethyl)phenyl)oxazole-2-carboxamide derivatives and the corresponding oxadiazole derivatives as usp30 inhibitors for the treatment of mitochondrial dysfunction
CA3185654A1 (en) 2020-06-04 2021-12-09 Mission Therapeutics Limited N-cyanopyrrolidines with activity as usp30 inhibitors
MX2022015608A (en) 2020-06-08 2023-03-03 Mission Therapeutics Ltd 1-(5-(2-cyanopyridin-4-yl)oxazole-2-carbonyl)-4-methylhexahydrop yrrolo[3,4-b]pyr role-5(1h)-carbonitrile as usp30 inhibitor for use in the treatment of mitochondrial dysfunction, cancer and fibrosis.
GB202016800D0 (en) 2020-10-22 2020-12-09 Mission Therapeutics Ltd Novel compounds
WO2023099561A1 (en) 2021-12-01 2023-06-08 Mission Therapeutics Limited Substituted n-cyanopyrrolidines with activity as usp30 inhibitors

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003530384A (en) 2000-04-06 2003-10-14 メルク フロスト カナダ アンド カンパニー Cathepsin cysteine protease inhibitor
AU2011305315A1 (en) * 2010-09-24 2013-03-28 The Regents Of The University Of Michigan Deubiquitinase inhibitors and methods for use of the same
EA026409B1 (en) 2011-10-19 2017-04-28 Виволюкс Аб Compound inhibiting deubiquitinating activity and use thereof in a composition and in a method of treating cancer
KR102204989B1 (en) * 2012-01-12 2021-01-20 예일 유니버시티 Compounds and Methods for the Enhanced Degradation of Targeted Proteins and Other Polypeptides by an E3 Ubiquitin Ligase
CA2927023C (en) 2013-10-10 2022-08-02 The Regents Of The University Of Michigan Deubiquitinase inhibitors and methods for use of the same
US9963444B2 (en) 2014-05-19 2018-05-08 Northeastern University N-acylethanolamine hydrolyzing acid amidase (NAAA) inhibitors and their use thereof
GB201416754D0 (en) 2014-09-23 2014-11-05 Mission Therapeutics Ltd Novel compounds
MD3277677T2 (en) * 2015-03-30 2021-07-31 Mission Therapeutics Ltd 1-cyano-pyrrolidine compounds as usp30 inhibitors
EP3322702B1 (en) 2015-07-14 2019-11-20 Mission Therapeutics Limited Cyanopyrrolidines as dub inhibitors for the treatment of cancer
GB201521109D0 (en) 2015-11-30 2016-01-13 Mission Therapeutics Ltd Novel compounds
GB201522267D0 (en) 2015-12-17 2016-02-03 Mission Therapeutics Ltd Novel compounds
GB201522768D0 (en) 2015-12-23 2016-02-03 Mission Therapeutics Ltd Novel compounds
GB201602854D0 (en) * 2016-02-18 2016-04-06 Mission Therapeutics Ltd Novel compounds
GB201603779D0 (en) 2016-03-04 2016-04-20 Mission Therapeutics Ltd Novel compounds
GB201604647D0 (en) 2016-03-18 2016-05-04 Mission Therapeutics Ltd Novel compounds
GB201604638D0 (en) 2016-03-18 2016-05-04 Mission Therapeutics Ltd Novel compounds
EP3433246B1 (en) 2016-03-24 2022-05-04 Mission Therapeutics Limited 1-cyano-pyrrolidine derivatives as dbu inhibitors
ES2850349T3 (en) 2016-09-27 2021-08-27 Mission Therapeutics Ltd Cyanopyrrolidine derivatives with activity as USP30 inhibitors
GB201616511D0 (en) 2016-09-29 2016-11-16 Mission Therapeutics Limited Novel compounds
GB201616627D0 (en) 2016-09-30 2016-11-16 Mission Therapeutics Limited Novel compounds
TWI771327B (en) 2016-10-05 2022-07-21 英商使命醫療公司 Novel compounds

Also Published As

Publication number Publication date
WO2017109488A8 (en) 2017-09-14
US10590075B2 (en) 2020-03-17
CN108290872A (en) 2018-07-17
CN108290872B (en) 2020-10-02
EP3394049A1 (en) 2018-10-31
EP3394049B1 (en) 2021-02-17
GB201522768D0 (en) 2016-02-03
JP6810148B2 (en) 2021-01-06
JP2019503362A (en) 2019-02-07
WO2017109488A1 (en) 2017-06-29

Similar Documents

Publication Publication Date Title
US10590075B2 (en) Cyanopyrrolidine derivatives as inhibitors for DUBs
US11319287B2 (en) Cyanopyrrolidines as dub inhibitors for the treatment of cancer
US11958833B2 (en) Compounds
US11236092B2 (en) Spiro-condensed pyrrolidine derivatives as deubiquitylating enzymes (DUB) inhibitors
US10927110B2 (en) Cyano-subtituted heterocycles with activity as inhibitors of USP30
US11084821B2 (en) Cyanopyrrolidine derivatives with activity as inhibitors of USP30
US11306096B2 (en) 4,6 dihydropyrrolo [3,4-C] pyrazole-5 (1H)-carbonitrile derivates for treating cancer
US10640498B2 (en) Compounds
US10683269B2 (en) 2-cyanoisoindoline derivatives for treating cancer
US11091488B2 (en) 1-cyano-pyrrolidine derivatives as inhibitors of USP30
US20210284631A1 (en) Cyano-substituted heterocycles with activity as inhibitors of usp30

Legal Events

Date Code Title Description
FEPP Fee payment procedure

Free format text: ENTITY STATUS SET TO UNDISCOUNTED (ORIGINAL EVENT CODE: BIG.); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

FEPP Fee payment procedure

Free format text: ENTITY STATUS SET TO SMALL (ORIGINAL EVENT CODE: SMAL); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

AS Assignment

Owner name: MISSION THERAPEUTICS LIMITED, GREAT BRITAIN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:KEMP, MARK IAN;WOODROW, MICHAEL DAVID;SIGNING DATES FROM 20180808 TO 20180904;REEL/FRAME:046778/0493

STPP Information on status: patent application and granting procedure in general

Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION

FEPP Fee payment procedure

Free format text: ENTITY STATUS SET TO UNDISCOUNTED (ORIGINAL EVENT CODE: BIG.); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: NOTICE OF ALLOWANCE MAILED -- APPLICATION RECEIVED IN OFFICE OF PUBLICATIONS

STPP Information on status: patent application and granting procedure in general

Free format text: PUBLICATIONS -- ISSUE FEE PAYMENT VERIFIED

STCF Information on status: patent grant

Free format text: PATENTED CASE

MAFP Maintenance fee payment

Free format text: PAYMENT OF MAINTENANCE FEE, 4TH YEAR, LARGE ENTITY (ORIGINAL EVENT CODE: M1551); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

Year of fee payment: 4